Associated Papers
Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene.
Savas S et al.
Genomics, 2004
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UK.
Blaydon DC et al.
Clinical Genetics, 2003
Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis.
Zwaenepoel I et al.
Human Mutation, 2001
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