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Gene Review

DFNB46  -  deafness, autosomal recessive 46

Homo sapiens

 
 
 
 
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High impact information on DFNB46

  • Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31 [1].

References

  1. Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31. Mir, A., Ansar, M., Chahrour, M.H., Pham, T.L., Wajid, M., Haque, S., Yan, K., Ahmad, W., Leal, S.M. Am. J. Med. Genet. A (2005) [Pubmed]
 
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