Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss

Ítems similars

• Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss
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• Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss
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• Identification of a novel POU4F3 frameshift variant in a Chinese family with autosomal dominant hearing loss
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• Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans
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• Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans
  per: He, Longxia, et al.
  Publicat: (2016)