Review of Genotype-Phenotype Correlations in Usher Syndrome-Reference-Cited by-同舟云学术

Review of Genotype-Phenotype Correlations in Usher Syndrome

Published:2021-05-25 Issue:1 Volume:43 Page:1-8
ISSN:1538-4667
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Nisenbaum Eric,Thielhelm Torin P.,Nourbakhsh Aida,Yan Denise,Blanton Susan H.,Shu Yilai,Koehler Karl R.,El-Amraoui Aziz,Chen Zhengyi,Lam Byron L.,Liu Xuezhong

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference101 articles.

1. Diversity of the genes implicated in algerian patients affected by usher syndrome.;Abdi;PLoS One,2016

2. The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.;Ahmed;J Neurosci,2006

3. Gene structure and mutant alleles of PCDH15: Nonsyndromic deafness DFNB23 and type 1 Usher syndrome.;Ahmed;Hum Genet,2008

4. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.;Ahmed;Am J Hum Genet,2001

5. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.;Ahmed;Hum Genet,2002

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