Clonal Cell Proliferation in Paroxysmal Nocturnal Hemoglobinuria: Evaluation of PIGA Mutations and T-cell Receptor Clonality-Reference-Cited by-同舟云学术

Clonal Cell Proliferation in Paroxysmal Nocturnal Hemoglobinuria: Evaluation of PIGA Mutations and T-cell Receptor Clonality

Published:2019-09-01 Issue:5 Volume:39 Page:438-446
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Park Joonhong¹²^ORCID,Kim Myungshin¹²^ORCID,Kim Yonggoo¹²^ORCID,Han Kyungja¹²^ORCID,Chung Nack-Gyun³^ORCID,Cho Bin³^ORCID,Lee Sung-Eun⁴^ORCID,Lee Jong Wook⁴^ORCID

Affiliation:

1. Department of Laboratory Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

2. Catholic Genetic Laboratory Center, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

3. Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Korea

4. Division of Hematology, Department of Internal Medicine, Catholic Blood and Marrow Transplantation Center, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

Funder

Ministry for Health, Welfare & Family Affairs

Ministry of Health and Welfare

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Link

https://synapse.koreamed.org/pdf/10.3343/alm.2019.39.5.438

Reference33 articles.

1. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene.

2. Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria