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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Publicat a:Am J Med Genet A
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2015
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Article
Accés en línia: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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