Novel mutations identified in known genes for autosomal recessive non-syndromic hearing loss (ARNSHL) in the current study.
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资源简介：
Acc. No., accession number of reference sequence; Chr, chromosome; Ex, exon; EVS, exome variant server; hg19, human genome assembly 19; In, intron; NA, not applicable; ND, not determined; SNPs, single nucleotide polymorphisms; PhyloP, phylogenetic P-values; Polyphen, polymorphism phenotyping; SIFT, sorting intolerance from tolerance.
创建时间：
2014-06-20
