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A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease)
Author(s) -
FaiyazUlHaque M,
AlJefri A,
Abalkhail HA,
Toulimat M,
AlMuallimi MA,
Pulicat MS,
Gaafar A,
Alaiya AA,
AlDayel F,
Peltekova I,
Zaidi SHE
Publication year - 2009
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2009.01244.x
Subject(s) - medicine , neutropenia , research centre , medical laboratory , family medicine , university hospital , pediatrics , library science , pathology , toxicity , computer science