(Q28264560)

5

object named as

T B Friedman

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author name string

X C Li

1

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L A Everett

2

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A K Lalwani

3

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D Desmukh

4

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E R Wilcox

https://scigraph.springernature.com/pub.10.1038/ng0398-215

7

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language of work or name

English

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publication date

March 1998

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published in

Nature Genetics

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volume

18

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page(s)

215-7

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issue

3

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exact match

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cites work

A type VII myosin encoded by the mouse deafness gene shaker-1

1 reference

https://api.crossref.org/works/10.1038/NG0398-215

Technetium-99m chelators in nuclear medicine. A review

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

Deafness with sporadic goiter. Pendred's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0398-215

1 reference

7 January 2021

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

7 January 2021

Pendred's syndrome. Acoustic, vestibular and radiological findings in 17 unrelated patients.

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

7 January 2021

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

7 January 2021

Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0398-215

7 January 2021

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/10.1038%2FNG0398-215

7 January 2021