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Novel mutations identified in known genes for autosomal recessive non-syndromic hearing loss (ARNSHL) in the current study.

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Figshare2015-12-02 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_Novel_mutations_identified_in_known_genes_for_autosomal_recessive_non_syndromic_hearing_loss_ARNSHL_in_the_current_study_/1065020
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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.
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2015-12-02
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