Did the GJB2 35delG Mutation Originate in Iran?

Mutations in GJB2 are a major cause of autosomal recessive non-syndromic hearing loss (ARNSHL) in many populations. A single mutation of this gene (35delG) accounts for approximately 70% of GJB2 mutations that are associated with ARNSHL in Caucasians in many European countries and also in Iranian. I...

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Bibliografiset tiedot
Julkaisussa:Am J Med Genet A
Päätekijät: Norouzi, Vahideh, Azizi, Hiva, Esteghamat, Fatemehsadat, Bazazzadegan, Niloofar, Fattahi, Zohreh, Nishimura, Carla, Nikzat, Nooshin, Jalalvand, Khadijeh, Kahrizi, Kimia, Smith, Richard. J. H., Najmabadi, Hossein
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4432473/
https://ncbi.nlm.nih.gov/pubmed/21910243
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.34225
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