Associations Between TGFA/TGFB3/MSX1 Gene Polymorphisms and Congenital Non-Syndromic Hearing Impairment in a Chinese Population

BACKGROUND: The aim of this study was to investigate whether the TGFA/TGFB3/MSX1 gene polymorphisms and haplotypes lead to individual differences between congenital non-syndromic hearing impairment (NSHI) patients and normal people in a Chinese population and to analyze the risk factors for NSHI. MA...

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Detalles Bibliográficos
Autores principales: Du, Jihong, Deng, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2016
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930271/
https://www.ncbi.nlm.nih.gov/pubmed/27356075
http://dx.doi.org/10.12659/MSM.896527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930271/
https://www.ncbi.nlm.nih.gov/pubmed/27356075
http://dx.doi.org/10.12659/MSM.896527

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