High-resolution melting analysis for detection of MYH9 mutations (Q33381637)

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title

High-resolution melting analysis for detection of MYH9 mutations (English)

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6

Ingrid Hrachovinova

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Dana Provaznikova

1

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Tereza Kumstyrova

2

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Roman Kotlin

3

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Peter Salaj

4

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Vaclav Matoska

5

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Simon Rittich

7

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publication date

1 September 2008

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volume

19

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issue

6

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page(s)

471-475

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Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes

26 July 2017

cites work

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https://api.crossref.org/works/10.1080%2F09537100802140013

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/10.1080%2F09537100802140013

Inherited giant platelet disorders. Classification and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F09537100802140013

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/10.1080%2F09537100802140013

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F09537100802140013

10.1080/09537100802140013

21 January 2018

Identifiers

DOI

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26 July 2017

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