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