(Q24539193)

English

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome

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scholarly article

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Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome (English)

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1 reference

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author name string

X Z Liu

1

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C Hope

2

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J Walsh

3

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V Newton

4

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X M Ke

5

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C Y Liang

6

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L R Xu

7

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J M Zhou

8

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D Trump

9

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K P Steel

10

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S Bundey

11

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S D Brown

12

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language of work or name

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publication date

September 1998

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American Journal of Human Genetics

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63

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3

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909-12

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Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B

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https://api.crossref.org/works/10.1086%2F302026

7 January 2021

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Conservation within the myosin motor domain: implications for structure and function

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

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Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

inferred from DOI database lookup

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

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Phenotypic diversity, allelic series and modifier genes

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

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Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

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Mutation analysis of the mouse myosin VIIA deafness gene

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

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Unconventional myosins, the basis for deafness in mouse and man.

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

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Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

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Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

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Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

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Usher syndrome in the city of Birmingham--prevalence and clinical classification

1 reference

https://api.crossref.org/works/10.1086%2F302026

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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