Table S1 - Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS
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https://figshare.com/articles/dataset/_Massively_Parallel_DNA_Sequencing_Successfully_Identifies_New_Causative_Mutations_in_Deafness_Genes_in_Patients_with_Cochlear_Implantation_and_EAS_/818760
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资源简介：
58 genes reported to be causative of non-syndromic hearing loss.
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创建时间：
2013-10-09
