A Boy with X-Linked Inhibitor of Apoptosis Protein (XIAP) Deficiency as the Initial Presentation of Pure Red Cell Aplasia-Reference-Cited by-同舟云学术

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A Boy with X-Linked Inhibitor of Apoptosis Protein (XIAP) Deficiency as the Initial Presentation of Pure Red Cell Aplasia

Published:2021-10-31 Issue:2 Volume:28 Page:84-88
ISSN:2233-5250
Container-title:Clinical Pediatric Hematology-Oncology
language:en
Short-container-title:Clin Pediatr Hematol Oncol

Author:

Sim Soo Yeun¹,Choi Hye Yeon¹,Han Seung Bum¹,Chung Nack Gyun¹,Cho Bin¹,Kim MyungShin²,Jeong Dae Chul¹^ORCID

Affiliation:

1. Department of Pediatrics, Catholic Genetic Laboratory Center, College of Medicine, The Catholic University of Korea, Seoul, Korea

2. Department of Laboratory Medicine, Catholic Genetic Laboratory Center, College of Medicine, The Catholic University of Korea, Seoul, Korea

Publisher

The Korean Society of Pediatric Hematology-Oncology

Subject

General Materials Science

Link

http://pdf.medrang.co.kr/CPHO/2021/028/CPHO028-02-84.pdf

Reference15 articles.

1. XIAP deficiency syndrome in humans

2. XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease

3. X-linked lymphoproliferative syndromes: brothers or distant cousins?

5. X-linked Inhibitor of Apoptosis Protein Deficiency: More than an X-linked Lymphoproliferative Syndrome

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