<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>158(1)</volume><submitter>Smith BN</submitter><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust</funding><journal>British journal of haematology</journal><pagination>146-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4533883</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia.</pubmed_title><pmcid>PMC4533883</pmcid><funding_grant_id>NF-SI-0507-10370</funding_grant_id><funding_grant_id>088683</funding_grant_id><pubmed_authors>Gale RE</pubmed_authors><pubmed_authors>Smith BN</pubmed_authors><pubmed_authors>Kaya Z</pubmed_authors><pubmed_authors>Segal AW</pubmed_authors><pubmed_authors>Hall G</pubmed_authors><pubmed_authors>Linch DC</pubmed_authors><pubmed_authors>Shakoori AR</pubmed_authors><pubmed_authors>Ali A</pubmed_authors><pubmed_authors>Evans C</pubmed_authors><pubmed_authors>Ancliff PJ</pubmed_authors><pubmed_authors>Hayee B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia.</name><description/><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Jul</publication><modification>2025-04-05T09:00:54.162Z</modification><creation>2025-04-05T09:00:54.162Z</creation></dates><accession>S-EPMC4533883</accession><cross_references><pubmed>22469094</pubmed><doi>10.1111/j.1365-2141.2012.09110.x</doi></cross_references></HashMap>