Associated Papers
Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome.
Krawitz PM et al.
Molecular Genetics & Genomic Medicine, 2014
Nonsyndromic hearing loss caused by USH1G mutations: widening the USH1G disease spectrum.
Maria Oonk AM et al.
Ear and Hearing, 0
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