Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria-Reference-Cited by-同舟云学术

Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria

Published:2014-09-17 Issue:10 Volume:124 Page:4529-4538
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Shen Wenyi,Clemente Michael J.,Hosono Naoko,Yoshida Kenichi,Przychodzen Bartlomiej,Yoshizato Tetsuichi,Shiraishi Yuichi,Miyano Satoru,Ogawa Seishi,Maciejewski Jaroslaw P.,Makishima Hideki

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference48 articles.

1. Paroxysmal Nocturnal Hemoglobinuria: Stem Cells and Clonality

2. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

3. Current concepts in the pathophysiology and treatment of aplastic anemia

4. Impaired Hematopoiesis in Paroxysmal Nocturnal Hemoglobinuria/Aplastic Anemia Is Not Associated With a Selective Proliferative Defect in the Glycosylphosphatidylinositol-Anchored Protein-Deficient Clone

5. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals

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