The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene (Q28589565)

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English	The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene	scientific journal article

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scholarly article

1 reference

31 January 2017

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene (English)

1 reference

31 January 2017

Protocadherin 15

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GOA release 2020-03-11

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based on heuristic

inferred from title

Richard P Woychik

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ORCID Public Data File 2021

author name string

K. N. Alagramam

1

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31 January 2017

C. L. Murcia

2

1 reference

31 January 2017

H. Y. Kwon

3

1 reference

31 January 2017

K. S. Pawlowski

4

1 reference

31 January 2017

C. G. Wright

5

1 reference

31 January 2017

R. P. Woychik

6

1 reference

31 January 2017

language of work or name

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publication date

1 January 2001

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31 January 2017

Nature Genetics

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31 January 2017

27

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31 January 2017

1

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31 January 2017

99–102

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31 January 2017

The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

1 reference

https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Identifying the genes of hearing, deafness, and dysequilibrium

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Genetic causes of hearing loss

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Electron Microscopic Studies of Capillary Permeability in Normal and Ames Waltzer Deaf Mice

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

based on heuristic

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Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Structural and functional diversity of cadherin superfamily: are new members of cadherin superfamily involved in signal transduction pathway?

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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A unique variant of a homeobox gene related to Drosophila cut is expressed in mouse testis.

1 reference

https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

1 reference

https://api.crossref.org/works/10.1038%2F83837

7 January 2021

based on heuristic

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Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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WWW-query: an on-line retrieval system for biological sequence banks

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https://api.crossref.org/works/10.1038%2F83837

7 January 2021

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Molecular characterization of the mouse agouti locus.

1 reference

https://api.crossref.org/works/10.1038%2F83837

7 January 2021

based on heuristic

inferred from DOI database lookup

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