The First Korean Case of Griscelli Syndrome Type 2 With Hemophagocytic Lymphohistiocytosis and Partial Albinism-Reference-Cited by-同舟云学术

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The First Korean Case of Griscelli Syndrome Type 2 With Hemophagocytic Lymphohistiocytosis and Partial Albinism

Published:2022-05-01 Issue:3 Volume:42 Page:384-388
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Lee Youngeun¹^ORCID,Park Hyun Jin²^ORCID,Kang Hyoung Jin²^ORCID,Ko Jung Min²^ORCID,Kim Boram¹^ORCID,Chang Yoon Hwan¹^ORCID,Kim Hyun Kyung¹^ORCID,Lee Jee-Soo¹^ORCID,Kim Man Jin¹^ORCID,Park Sung Sup¹³^ORCID,Seong Moon-Woo¹³^ORCID

Affiliation:

1. Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea

2. Department of Pediatrics, Seoul National University Children’s Hospital, Seoul National University College of Medicine, Seoul, Korea

3. Biomedical Research Institute, Seoul National University Hospital, Seoul, Korea

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

http://pdf.medrang.co.kr/ALM/2022/042/ALM042-03-384.pdf

Reference10 articles.

1. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis

2. INFECTION- AND MALIGNANCY-ASSOCIATED HEMOPHAGOCYTIC SYNDROMES

3. A syndrome associating partial albinism and immunodeficiency

4. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

5. Further evidence for genotype-phenotype disparity in Griscelli syndrome

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