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Article

Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia.

Thrombosis and haemostasis - 1 Oct 2010

Fabris Fabrizio, Scandellari Raffaella, Vettore Silvia, Scapin Margherita, Bizzaro Nicola, Randi Maria L

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Identifiers

PMID: 20694274
DOI: 10.1160/TH10-01-0041

Genes

MYH9

Provenance

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Related research

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Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia.PMID 20694274Read ↗

[MYH9-related macrothrombocytopenia].Semantic proximity Read ↗

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

A D1424N mutation in the MYH9 gene results in macrothrombocytopenia and granulocytic inclusion bodies in a Chinese inherited macrothrombocytopenia pedigree.Semantic proximity Read ↗

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

A De Novo Mutation in MYH9 in a Child With Severe and Prolonged Macrothrombocytopenia.Semantic proximity Read ↗

MYH9 disorder: Identification and a novel mutation in patients with macrothrombocytopenia.Semantic proximity Read ↗

MYH-9 Related Platelet Disorders: Strategies for Management and DiagnosisSemantic proximity Read ↗

Successful living-related kidney transplantation in MYH9-related disorder with macrothrombocytopenia: lessons for the clinical nephrologist.Semantic proximity Read ↗

Paris-Trousseau-type macrothrombocytopenia without 11q deletion.Semantic proximity Read ↗

[MYH9 syndrome and auto-immune haemolytic anaemia: an unrelated association?].Semantic proximity Read ↗

MYH9-Related Platelet DisordersSemantic proximity Read ↗

Progress in understanding the diagnosis and molecular genetics of macrothrombocytopeniasSemantic proximity Read ↗

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