<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(1-2)</volume><submitter>Leigh MW</submitter><funding>NCATS NIH HHS</funding><funding>NHLBI NIH HHS</funding><journal>Translational science of rare diseases</journal><pagination>51-75</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6768089</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Primary Ciliary Dyskinesia (PCD): A genetic disorder of motile cilia.</pubmed_title><pmcid>PMC6768089</pmcid><funding_grant_id>UL1 TR002489</funding_grant_id><funding_grant_id>R01 HL071798</funding_grant_id><funding_grant_id>U2C TR002818</funding_grant_id><funding_grant_id>U54 HL096458</funding_grant_id><pubmed_authors>O'Connor MG</pubmed_authors><pubmed_authors>Knowles MR</pubmed_authors><pubmed_authors>Horani A</pubmed_authors><pubmed_authors>Kinghorn B</pubmed_authors><pubmed_authors>Zariwala MA</pubmed_authors><pubmed_authors>Leigh MW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Primary Ciliary Dyskinesia (PCD): A genetic disorder of motile cilia.</name><description/><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2025-04-26T06:12:24.05Z</modification><creation>2025-04-06T11:45:02.767Z</creation></dates><accession>S-EPMC6768089</accession><cross_references><pubmed>31572664</pubmed><doi>10.3233/TRD-190036</doi><doi>10.3233/trd-190036</doi></cross_references></HashMap>