Recurrent mutations in known autosomal recessive non-syndromic hearing loss (ARNSHL) genes in 6 Pakistani families.
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数据链接：
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资源简介：
Acc. No., accession number of reference sequence; Chr, chromosome; Ex, exon; EVS, exome variant server; In, intron; SNPs, single nucleotide polymorphisms; Ref, references.
创建时间：
2014-06-20
