No abstract available
Publication types
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Letter
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adult
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Aged
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Europe, Eastern / ethnology
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Female
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Genotype
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Hearing Loss, Sensorineural* / diagnosis
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Hearing Loss, Sensorineural* / ethnology
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Hearing Loss, Sensorineural* / genetics
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Homozygote
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Humans
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Jews / genetics*
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Male
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Membrane Proteins / genetics
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Middle Aged
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Mutation
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Pedigree
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Phenotype
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Retinitis Pigmentosa* / diagnosis
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Retinitis Pigmentosa* / ethnology
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Retinitis Pigmentosa* / genetics
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Syndrome
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Vestibular Diseases* / diagnosis
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Vestibular Diseases* / ethnology
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Vestibular Diseases* / genetics
Substances
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CLRN1 protein, human
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Membrane Proteins
Associated data
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OMIM/276900
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OMIM/276901
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OMIM/276902
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OMIM/276903
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OMIM/276904
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OMIM/276905
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OMIM/601067
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OMIM/602083
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OMIM/602097
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OMIM/605472
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OMIM/606943