PDZD7 and hearing loss: more than just a modifier

Deafness is the most frequent sensory disorder. With over 90 genes and 110 loci causally implicated in non-syndromic hearing loss, it is phenotypically and genetically heterogeneous. Here we investigate the genetic etiology of deafness in four families of Iranian origin segregating autosomal recessi...

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Detalhes bibliográficos
Publicado no:Am J Med Genet A
Main Authors: Booth, Kevin T, Azaiez, Hela, Kahrizi, Kimia, Simpson, Allen C, Tollefson, William TA, Sloan, Christina M, Meyer, Nicole C, Babanejad, Mojgan, Ardalani, Fariba, Arzhangi, Sanaz, Schnieders, Michael J, Najmabadi, Hossein, Smith, Richard JH
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4741280/
https://ncbi.nlm.nih.gov/pubmed/26416264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.37274
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