Spectrum of recurrent GJB2 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss (ARNSHL).
收藏Figshare2015-12-02 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_Spectrum_of_recurrent_GJB2_mutations_in_Pakistani_families_with_autosomal_recessive_non_syndromic_hearing_loss_ARNSHL_/1065019
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As reference sequence NM_004004.5 was employed. EVS, exome variant server;#The pathogenicity of this mutation is controversial.
创建时间:
2015-12-02



