Genetic heterogeneity in Usher syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference39 articles.
1. Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F
2. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
3. A Mutation ofPCDH15among Ashkenazi Jews with the Type 1 Usher Syndrome
4. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
5. Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle
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3. Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization;Communications Biology;2023-09-12
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