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Article

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

Pediatric blood & cancer - 1 Sept 2024

Yin Charles, Turley Elona, Livingston Joel

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Identifiers

PMID: 38965687
DOI: 10.1002/pbc.31183

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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Identification of a novel MYH9-related disease-associated mutation with multiple faintly staining Döhle-like bodies.PMID 38965687Read ↗

Description of a novel mutation leading to MYH9-related disease.Semantic proximity Read ↗

Unveiling the hidden clues: Döhle body-like inclusions as morphological markers for MYH9-related disorders: A case report.Semantic proximity Read ↗

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly.Semantic proximity Read ↗

Early diagnosis improves the quality of life in MYH9 disorder.Semantic proximity Read ↗

Understanding MYH-associated neoplasia.Semantic proximity Read ↗

A case report of a family with MYH9 gene mutation-related disease in an ethnic minority group and literature review.Semantic proximity Read ↗

OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH.Semantic proximity Read ↗

A case of MYH9 disorders caused by a novel mutation (p.K74E).Semantic proximity Read ↗

PNH phenotypes and their genesis.Semantic proximity Read ↗

Gene symbol: MYH7.Semantic proximity Read ↗

Gene symbol: MYH7.Semantic proximity Read ↗

Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents.Semantic proximity Read ↗

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