<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Chan KW</submitter><pubmed_abstract>To address inborn errors of immunity (IEI) which were underdiagnosed in resource-limited regions, our centre developed and offered free genetic testing for the most common IEI by Sanger sequencing (SS) since 2001. With the establishment of The Asian Primary Immunodeficiency (APID) Network in 2009, the awareness and definitive diagnosis of IEI were further improved with collaboration among centres caring for IEI patients from East and Southeast Asia. We also started to use whole exome sequencing (WES) for undiagnosed cases and further extended our collaboration with centres from South Asia and Africa. With the increased use of Next Generation Sequencing (NGS), we have shifted our diagnostic practice from SS to WES. However, SS was still one of the key diagnostic tools for IEI for the past t</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>883446</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9304939</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity.</pubmed_title><pmcid>PMC9304939</pmcid><pubmed_authors>Liang W</pubmed_authors><pubmed_authors>Vignesh P</pubmed_authors><pubmed_authors>Jouhadi Z</pubmed_authors><pubmed_authors>Muktiarti D</pubmed_authors><pubmed_authors>Latiff ZA</pubmed_authors><pubmed_authors>He JX</pubmed_authors><pubmed_authors>Suratannon N</pubmed_authors><pubmed_authors>Djidjik R</pubmed_authors><pubmed_authors>Isa MS</pubmed_authors><pubmed_authors>Belaid B</pubmed_authors><pubmed_authors>Jin R</pubmed_authors><pubmed_authors>Casis-Hao RJ</pubmed_authors><pubmed_authors>Vaughan J</pubmed_authors><pubmed_authors>Foronda R</pubmed_authors><pubmed_authors>Shek LP</pubmed_authors><pubmed_authors>Jindal AK</pubmed_authors><pubmed_authors>Camonayan KAB</pubmed_authors><pubmed_authors>Al-Saad K</pubmed_authors><pubmed_authors>Lee TL</pubmed_authors><pubmed_authors>Jiratchaya C</pubmed_authors><pubmed_authors>Fong SM</pubmed_authors><pubmed_authors>Wong WH</pubmed_authors><pubmed_authors>Kechout N</pubmed_authors><pubmed_authors>Mak PHS</pubmed_authors><pubmed_authors>Chong PCY</pubmed_authors><pubmed_authors>Zhao X</pubmed_authors><pubmed_authors>Urban M</pubmed_authors><pubmed_authors>Barbouche MR</pubmed_authors><pubmed_authors>Suri D</pubmed_authors><pubmed_authors>Yang XQ</pubmed_authors><pubmed_authors>Yeoh AEJ</pubmed_authors><pubmed_authors>Le MHT</pubmed_authors><pubmed_authors>Lobo RCM</pubmed_authors><pubmed_authors>Jirapongsananuruk O</pubmed_authors><pubmed_authors>Rawat A</pubmed_authors><pubmed_authors>Lee BW</pubmed_authors><pubmed_authors>Vera M</pubmed_authors><pubmed_authors>Phan Nguyen Lien A</pubmed_authors><pubmed_authors>Wongwaree S</pubmed_authors><pubmed_authors>Cheong KN</pubmed_authors><pubmed_authors>Yu HH</pubmed_authors><pubmed_authors>Duque JR</pubmed_authors><pubmed_authors>Chien YH</pubmed_authors><pubmed_authors>Binas VWE</pubmed_authors><pubmed_authors>Kamchaisatian W</pubmed_authors><pubmed_authors>Chen TX</pubmed_authors><pubmed_authors>Lau YL</pubmed_authors><pubmed_authors>Gupta A</pubmed_authors><pubmed_authors>Nguyen VAT</pubmed_authors><pubmed_authors>Lao-Araya M</pubmed_authors><pubmed_authors>Chan SY</pubmed_authors><pubmed_authors>Chan KW</pubmed_authors><pubmed_authors>Villanueva JCMM</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Singh S</pubmed_authors><pubmed_authors>Trakultivakorn M</pubmed_authors><pubmed_authors>Ho MHK</pubmed_authors><pubmed_authors>Wong CY</pubmed_authors><pubmed_authors>Yao L</pubmed_authors><pubmed_authors>Capulong RD</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Koh MT</pubmed_authors><pubmed_authors>Chan LL</pubmed_authors><pubmed_authors>Ismail IH</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Fok SFS</pubmed_authors><pubmed_authors>Lee AC</pubmed_authors><pubmed_authors>Tu W</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Mao H</pubmed_authors><pubmed_authors>Liew WK</pubmed_authors><pubmed_authors>Au EY</pubmed_authors><pubmed_authors>Chua GT</pubmed_authors><pubmed_authors>Wong KJ</pubmed_authors><pubmed_authors>Leung D</pubmed_authors><pubmed_authors>Ma W</pubmed_authors><pubmed_authors>Kwok JS</pubmed_authors><pubmed_authors>Phongsamart G</pubmed_authors><pubmed_authors>Lee PP</pubmed_authors><pubmed_authors>Hui WY</pubmed_authors><pubmed_authors>Raj R</pubmed_authors><pubmed_authors>Jiang LP</pubmed_authors><pubmed_authors>Santos-Ocampo FJ</pubmed_authors><pubmed_authors>Abdul Latiff AH</pubmed_authors><pubmed_authors>Chantveerawong T</pubmed_authors><pubmed_authors>de Silva R</pubmed_authors><pubmed_authors>Boushaki S</pubmed_authors><pubmed_authors>Raj D</pubmed_authors><pubmed_authors>Quynh Le NN</pubmed_authors><pubmed_authors>Ang EY</pubmed_authors><pubmed_authors>van den Berg S</pubmed_authors><pubmed_authors>Thong MK</pubmed_authors><pubmed_authors>Mallillin JM</pubmed_authors><pubmed_authors>Eley B</pubmed_authors><pubmed_authors>Lee WS</pubmed_authors><pubmed_authors>Noh LM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity.</name><description>To address inborn errors of immunity (IEI) which were underdiagnosed in resource-limited regions, our centre developed and offered free genetic testing for the most common IEI by Sanger sequencing (SS) since 2001. With the establishment of The Asian Primary Immunodeficiency (APID) Network in 2009, the awareness and definitive diagnosis of IEI were further improved with collaboration among centres caring for IEI patients from East and Southeast Asia. We also started to use whole exome sequencing (WES) for undiagnosed cases and further extended our collaboration with centres from South Asia and Africa. With the increased use of Next Generation Sequencing (NGS), we have shifted our diagnostic practice from SS to WES. However, SS was still one of the key diagnostic tools for IEI for the past t</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-25T18:09:51.76Z</modification><creation>2025-04-06T07:30:58.666Z</creation></dates><accession>S-EPMC9304939</accession><cross_references><pubmed>35874699</pubmed><doi>10.3389/fimmu.2022.883446</doi></cross_references></HashMap>