Associated Papers
Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants.
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Supplement: biology-12-00505-s001.zip › biology-2074814-supplementary.xlsx › Table_S1
Mutation analysis of common deafness genes among 1,201 patients with non-syndromic hearing loss in Shanxi Province.
Zhou Y et al.
Molecular Genetics & Genomic Medicine, 2019
The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem.
Taylor RA et al.
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Journal of Neuroscience Research, 2002
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