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Article

A case of MYH9 disorders caused by a novel mutation (p.K74E).

Annals of hematology - 1 Jan 2016

Kanematsu Takeshi, Suzuki Nobuaki, Yoshida Tadao, Kishimoto Mayuko, Aoki Tomohiro, Ogawa Mika, Kagami Yoshitoyo, Kiyoi Hitoshi, Matsushita Tadashi, Kunishima Shinji

Abstract excerpt

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Topics

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Share to MYH9 gene
Share to Molecular Motor Proteins
Share to Mutation
Share to Myosin Heavy Chains

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Protein Structure, Secondary

Share to Thrombocytopenia

Source

Identifiers

PMID: 26382273
DOI: 10.1007/s00277-015-2506-9

Genes

MYH9

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of MYH9 disorders caused by a novel mutation (p.K74E).PMID 26382273Read ↗

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

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

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

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

A rare case of MYH9 disorders presenting with macrothrombocytopenia and deafness caused by MYH9-R702C mutation.Semantic proximity Read ↗

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

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

Identification of the first in cis mutations in MYH9 disorder.Semantic proximity Read ↗

[Identification of MYH9 gene mutation in a May-Hegglin anomaly family].Semantic proximity Read ↗

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

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