Identification of a novel MYH9‐related disease‐associated mutation with multiple faintly staining Döhle‐like bodies-Reference-Cited by-同舟云学术

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Identification of a novel MYH9‐related disease‐associated mutation with multiple faintly staining Döhle‐like bodies

Published:2024-07-04 Issue:9 Volume:71 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Yin Charles¹²^ORCID,Turley Elona¹^ORCID,Livingston Joel³

Affiliation:

1. Division of Hematological Pathology Department of Laboratory Medicine and Pathology University of Alberta Edmonton Canada

2. Division of Experimental Oncology Department of Oncology University of Alberta Edmonton Canada

3. Division of Pediatric Hematology/Oncology Department of Pediatrics University of Alberta Edmonton Canada

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.31183

Reference13 articles.

1. MYH9-Related Platelet Disorders

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

3. A familial case of MYH9 gene mutation associated with multiple functional and structural platelet abnormalities

4. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes

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