A MAYAN FOUNDER MUTATION IS A COMMON CAUSE OF DEAFNESS IN GUATEMALA

Over 5% of the world population have varying degrees of hearing loss. Mutations in GJB2 are the most common cause of autosomal recessive non-syndromic hearing loss (NSHL) in many populations. The frequency and type of mutations are influenced by ethnicity. Guatemala is a multi-ethnic country with fo...

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Xehetasun bibliografikoak
Argitaratua izan da:Clin Genet
Egile Nagusiak: Carranza, Claudia, Menendez, Ibis, Herrera, Mariana, Castellanos, Patricia, Amado, Carlos, Maldonado, Fabiola, Rosales, Luisa, Escobar, Nancy, Guerra, Mariela, Alvarez, Darwin, Foster, Joseph, Guo, Shengru, Blanton, Susan H., Bademci, Guney, Tekin, Mustafa
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2015
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5484753/
https://ncbi.nlm.nih.gov/pubmed/26346709
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12676
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