A Case of Myosin-heavy-chain-9 (MYH9) Gene Mutation Confirmed May-Hegglin Anomaly: 11-year Follow-up-Reference-Cited by-同舟云学术

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A Case of Myosin-heavy-chain-9 (MYH9) Gene Mutation Confirmed May-Hegglin Anomaly: 11-year Follow-up

Published:2016-10-31 Issue:2 Volume:23 Page:167-170
ISSN:2233-5250
Container-title:Clinical Pediatric Hematology-Oncology
language:en
Short-container-title:Clin Pediatr Hematol Oncol

Author:

Park Seong Jun¹,Wy Hwahyun¹,Jung Hye Lim¹^ORCID,Shim Jae Won¹,Shim Jung Yeon¹,Kim Deok Soo¹,Park Moon Soo¹,Seo Soo Hyun²,Seong Moon Woo³

Affiliation:

1. Department of Pediatrics, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea

2. Department of Laboratory Medicine, Seoul National University Boramae Medical Center, Seoul National University College of Medicine, Seoul, Korea

3. Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea

Publisher

The Korean Society of Pediatric Hematology-Oncology

Subject

General Materials Science

Link

http://pdf.medrang.co.kr/CPHO/2016/023/CPHO023-02-13.pdf

Reference12 articles.

1. R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura

2. MYH-9 Related Platelet Disorders: Strategies for Management and Diagnosis

3. Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias

4. Clinical, Pathological, and Genetic Analysis of Ten Patients with MYH9-Related Disease

5. MYH9-Related Platelet Disorders

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Case of Thrombocytopenia with <italic>MYH9</italic> Gene Mutation Found in Siblings;Soonchunhyang Medical Science;2024-06-30

2. Neonatal Thrombocytopenia due to MYH9 Missense Mutation: A Case Report;Perinatology;2022

3. Genetic classification and confirmation of inherited platelet disorders: current status in Korea;Clinical and Experimental Pediatrics;2020-03-15

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