Related references
Note: Only part of the references are listed.Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
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Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans
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Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome:: low prevalence and phenotypic variability
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JOURNAL OF MEDICAL GENETICS (2003)
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ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY (2003)
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GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY (2002)
USH3A transcripts encode clarin-1, a four- transmembrane-domain protein with a possible role in sensory synapses
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AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder
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