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usher syndrome, type 1d
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CDH23
Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
Prediction of the Coding Sequences of Unidentified Human Genes. XX. The Complete Sequences of 100 New cDNA Clones from Brain Which Code for Large Proteins in vitro
PCDH15
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
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