Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria

Paroxysmal nocturnal hemoglobinuria (PNH) is a nonmalignant clonal disease of hematopoietic stem cells that is associated with hemolysis, marrow failure, and thrombophilia. PNH has been considered a monogenic disease that results from somatic mutations in the gene encoding PIGA, which is required fo...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Shen, Wenyi, Clemente, Michael J., Hosono, Naoko, Yoshida, Kenichi, Przychodzen, Bartlomiej, Yoshizato, Tetsuichi, Shiraishi, Yuichi, Miyano, Satoru, Ogawa, Seishi, Maciejewski, Jaroslaw P., Makishima, Hideki
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society for Clinical Investigation 2014
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4191017/
https://ncbi.nlm.nih.gov/pubmed/25244093
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI74747
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg