(Q33373973)

26 July 2017

title

Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations (English)

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26 July 2017

Shinji Kunishima

1

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26 July 2017

Miyako Yoshinari

2

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26 July 2017

Hisanori Nishio

3

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26 July 2017

Komei Ida

4

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26 July 2017

Takuma Miura

5

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26 July 2017

Tadashi Matsushita

6

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26 July 2017

Motohiro Hamaguchi

7

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26 July 2017

Hidehiko Saito

8

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26 July 2017

publication date

16 January 2007

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European Journal of Haematology

26 July 2017

published in

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26 July 2017

volume

78

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26 July 2017

issue

3

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26 July 2017

page(s)

220-226

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Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.

26 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly): clinical and laboratory findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Misdiagnosis of chronic thrombocytopenia in childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

A unique immunofluorescence method promotes accurate diagnosis in MYH9 disorders: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Genotype-phenotype correlation in MYH9-related thrombocytopenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Hereditary macrothrombocytopathia, nephritis and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Mapping of a gene for May-Hegglin anomaly to chromosome 22q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

Crystal structure of a vertebrate smooth muscle myosin motor domain and its complex with the essential light chain: visualization of the pre-power stroke state

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0609.2006.00806.X

10.1111/J.1600-0609.2006.00806.X

21 January 2018

Identifiers

DOI

1 reference

26 July 2017

1 reference