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Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia
Journal article   Peer reviewed

Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia

Bradley N. Smith, Catherine Evans, Akbar Ali, Phil J. Ancliff, Bu'Hussain Hayee, Anthony W. Segal, Georgina Hall, Zuhre Kaya, Abdul Rauf Shakoori, David C. Linch, …
British journal of haematology, Vol.158(1), pp.146-149
07/2012
PMCID: PMC4533883
PMID: 22469094

Abstract

DNA mutation G6PC3 molecular diagnosis recessive severe congenital neutropenia

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