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t/gene-myh9

MYH9 gene

Discuss publications and research concerning the MYH9 gene.

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Related literature

Research Advances in the Physiological and Pathological Function of MYH9 and NMIIA.
MYH9
A case report of a family with MYH9 gene mutation-related disease in an ethnic minority group and literature review.
MYH9
Biological findings from the PheWAS catalog: focus on connective tissue-related disorders (pelvic floor dysfunction, abdominal hernia, varicose veins and hemorrhoids).
MYH9
Association of MYH9 rs3752462 and rs5756168 Polymorphisms With Transplanted Kidney Artery Stenosis.
MYH9
A case of MYH9 disorders caused by a novel mutation (p.K74E).
MYH9
Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals.
MYH9
Crystal structure of the rigor-like human non-muscle myosin-2 motor domain.
MYH9
[MYH9-related macrothrombocytopenia].
MYH9
R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura.
MYH9
[Hereditary sensorineural hearing impairment and macrothrombocytopenia: a rare MYH9 gene mutation].
MYH9

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