The Phenotype of a Germline Mutation in PIGA: The Gene Somatically Mutated in Paroxysmal Nocturnal Hemoglobinuria-Reference-Cited by-同舟云学术

The Phenotype of a Germline Mutation in PIGA: The Gene Somatically Mutated in Paroxysmal Nocturnal Hemoglobinuria

Published:2012-02 Issue:2 Volume:90 Page:295-300
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Johnston Jennifer J.,Gropman Andrea L.,Sapp Julie C.,Teer Jamie K.,Martin Jodie M.,Liu Cyndi F.,Yuan Xuan,Ye Zhaohui,Cheng Linzhao,Brodsky Robert A.,Biesecker Leslie G.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Inherited glycosylphosphatidyl inositol deficiency: A treatable CDG;Almeida;Biochim. Biophys. Acta,2009

2. Narrative review: paroxysmal nocturnal hemoglobinuria: the physiology of complement-related hemolytic anemia;Brodsky;Ann. Intern. Med.,2008

3. How I treat paroxysmal nocturnal hemoglobinuria;Brodsky;Blood,2009

4. Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria;Ware;Blood,1994

5. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene;Bessler;EMBO J.,1994

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