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Article

A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation.

Hematology (Amsterdam, Netherlands) - 1 Dec 2020

Zhang Wenchao, Lian Xiaoqiang, Sun Yifeng, Hao Jihong

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Identifiers

PMID: 31888422
DOI: 10.1080/16078454.2019.1706808

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Related research

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A sporadic MYH9-related disease in a Chinese boy with p.A95T mutation.PMID 31888422Read ↗

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

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

A novel MYH9 variant in a Chinese patient with MYH9 related diseaseSemantic proximity Read ↗

Novel variant of MYH9 associated with mild evaluation of MYH9 related disorder in a Chinese family.Semantic proximity Read ↗

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A Japanese pedigree with a p.A95V mutation in the MYH9 gene demonstrates inherited macrothrombocytopenia without Alport manifestations.Semantic proximity Read ↗

Transient hemiparesis in a 14-year-old boy with MYH9 disorders.Semantic proximity Read ↗

[Mutation analysis for a large Chinese family affected with MYH9-related thrombocytopenia].Semantic proximity Read ↗

A novel deletion mutation of ATP7A gene in a Chinese family with Menkes disease.Semantic proximity Read ↗

A novel A allele with c.499G>A mutation identified in a Chinese individual.Semantic proximity Read ↗

[Gene analysis and clinical features of MYH9-related disease].Semantic proximity Read ↗

Adams-Oliver syndrome and familial MYH9 mutation.Semantic proximity Read ↗

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