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

31 January 2017

title

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

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ORCID Public Data File 2021

31 January 2017

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GOA release 2020-03-11

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author name string

K. N. Alagramam

1

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31 January 2017

C. L. Murcia

2

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31 January 2017

H. Y. Kwon

3

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31 January 2017

K. S. Pawlowski

4

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31 January 2017

C. G. Wright

5

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31 January 2017

R. P. Woychik

6

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31 January 2017

language of work or name

English

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publication date

1 January 2001

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31 January 2017

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31 January 2017

volume

27

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31 January 2017

issue

1

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31 January 2017

page(s)

99–102

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

31 January 2017

cites work

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7 January 2021

Identifying the genes of hearing, deafness, and dysequilibrium

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7 January 2021

Genetic causes of hearing loss

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

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7 January 2021

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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7 January 2021

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

1 reference

7 January 2021

Molecular characterization of the mouse agouti locus.

1 reference

7 January 2021