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Article

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

Hearing research - 1 Jun 2003

Hampton Lori L, Wright Charles G, Alagramam Kumar N, Battey James F, Noben-Trauth Konrad

Abstract excerpt

A recessive deafness mutation in the mouse arose spontaneously and was identified in a colony segregating a null allele of the gastrin-releasing peptide receptor (Grpr) locus. Auditory-evoked brain stem response measurements revealed deafness in 7-week-old affected mice. By linkage analyses, the mutant phenotype was mapped near marker D10Mit186 and the protocadherin gene Pcdh15. As shown by complementation...

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Source

Identifiers

PMID: 12782354
DOI: 10.1016/s0378-5955(03)00107-2

Genes

PCDH15

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.PMID 12782354Read ↗

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