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2011
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2002
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2000
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Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
Not available
S-EPMC1287932
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biostudies-literature
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CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.
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S-EPMC379159
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biostudies-literature
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Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
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S-EPMC3035704
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biostudies-literature
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