关键词: Vohwinkel syndrome ainhum connexin 26 mutilating palmoplantar keratoderma sensorineural deafness
Mesh : Abnormalities, Multiple / genetics Adult Asians Connexin 26 Connexins / genetics Female Hand Deformities, Congenital / genetics Hearing Loss, Sensorineural / genetics Humans Keratoderma, Palmoplantar / genetics Mutation, Missense
来 源:
DOI:10.1111/1346-8138.14727
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