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Gene Review

DFN6  -  deafness, X-linked 6, sensorineural

Homo sapiens

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High impact information on DFN6


  1. A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22. del Castillo, I., Villamar, M., Sarduy, M., Romero, L., Herraiz, C., Hernández, F.J., Rodríguez, M., Borrás, I., Montero, A., Bellón, J., Tapia, M.C., Moreno, F. Hum. Mol. Genet. (1996) [Pubmed]
  2. Clinical phenotype of DFN2, DFN4 and DFN6. Pfister, M.H., Lalwani, A.K. Adv. Otorhinolaryngol. (2002) [Pubmed]
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