(Q28239757)

1

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P Küssel

2

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S Blanchard

3

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G Lévy

4

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F Levi-Acobas

5

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M Drira

6

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H Ayadi

https://scigraph.springernature.com/pub.10.1038/ng0697-191

7

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language of work or name

English

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publication date

June 1997

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published in

Nature Genetics

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volume

16

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page(s)

191-3

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issue

2

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exact match

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cites work

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

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

21 April 2017

1 reference

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 April 2017

1 reference

Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia

21 April 2017

1 reference

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

21 April 2017

1 reference

Cloning, analysis, and chromosomal localization of myoxin (MYH12), the human homologue to the mouse dilute gene

21 April 2017

1 reference

Mammalian Ras interacts directly with the serine/threonine kinase Raf

21 April 2017

1 reference

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells

21 April 2017

1 reference

A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene

21 April 2017

1 reference

Genes responsible for human hereditary deafness: symphony of a thousand

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Localization of two genes for Usher syndrome type I to chromosome 11.

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

A 5' splice-region G----C mutation in exon 1 of the human beta-globin gene inhibits pre-mRNA splicing: a mechanism for beta+-thalassemia

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Ehlers-Danlos Syndrome Type IV: A Single Base Substitution of the Last Nucleotide of Exon 34 in COL3A1 Leads to Exon Skipping

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Two novel splicing mutations in the XPA gene in patients with group A xeroderma pigmentosum

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

A simple method for displaying the hydropathic character of a protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Three-dimensional structure of myosin subfragment-1: a molecular motor

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Brain myosin-V is a two-headed unconventional myosin with motor activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021

Expression of myosin VIIA during mouse embryogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-191

7 January 2021