Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23
Top Cited Papers
- 1 January 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (1) , 26-37
- https://doi.org/10.1086/316954
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members 1 1Edited by M. YanivJournal of Molecular Biology, 2000
- Recent progress in hereditary hearing lossCurrent Opinion in Otolaryngology & Head and Neck Surgery, 1999
- Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessNature Genetics, 1997
- A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21Human Molecular Genetics, 1997
- Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22Human Molecular Genetics, 1996
- Faster Linkage Analysis Computations for Pedigrees with Loops or Unused AllelesHuman Heredity, 1996
- Defective myosin VIIA gene responsible for Usher syndrome type IBNature, 1995
- Linkage of usher syndrome type I gene (USH1B) to the long arm of chromosome 11Genomics, 1992
- A gene for usher syndrome type I (USH1A) maps to chromosome 14qGenomics, 1992
- Localization of two genes for usher syndrome type I to chromosome 11Genomics, 1992