Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Gene Review:

DFN6 - deafness, X-linked 6, sensorineural

Homo sapiens

This record was replaced with 23676.

del Castillo, I. et al., Pfister, M.H. et al.

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High impact information on DFN6

A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22 [1].
The position of the novel deafness locus (DFN6) was refined by haplotype analysis [1].
Clinical phenotype of DFN2, DFN4 and DFN6 [2].

References

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]
Clinical phenotype of DFN2, DFN4 and DFN6. Pfister, M.H., Lalwani, A.K. Adv. Otorhinolaryngol. (2002) [Pubmed]

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