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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Query Trace: Hearing and DMXL2[original query]
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family.
Experimental biology and medicine (Maywood, N.J.) 2021 Mar 1535370221999746.
Wonkam-Tingang Edmond, Schrauwen Isabelle, Esoh Kevin K, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Nasir Abdul, Leal Suzanne M, Wonkam Ambroi
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