(Q44462859)

3 December 2017

title

A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15. (English)

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3 December 2017

Lori L Hampton

1

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3 December 2017

Charles G Wright

2

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3 December 2017

Kumar N Alagramam

3

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3 December 2017

James F Battey

4

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3 December 2017

Konrad Noben-Trauth

5

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3 December 2017

publication date

1 June 2003

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3 December 2017

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3 December 2017

volume

180

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3 December 2017

issue

1-2

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3 December 2017

page(s)

67-75

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Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

3 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v).

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

Loss of bombesin-induced feeding suppression in gastrin-releasing peptide receptor-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

Specificity of cell adhesion in development: the cadherin superfamily

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

Recent progress in protocadherin research

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2803%2900107-2

7 January 2021

10.1016/S0378-5955(03)00107-2

Identifiers

DOI

1 reference

3 December 2017

1 reference