Case–Control Genotyping of the c.788C>T Variant of Transforming Growth Factor-Beta 1 Gene in Otosclerosis in the South Indian Population

Background: Otosclerosis is a common conductive hearing loss resulting from abnormal bone metabolism. The c.788C>T variant in the transforming growth factor-beta 1 gene is associated with otosclerosis in all studied populations, except the Indian population. In this study, we predicted the functi...

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Detalles Bibliográficos
Autores principales: Kale, Deepa, Rekha, Santhanam, Vinoth, Sigamani, Ramalingam, Ravi, Parani, Madasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Academy of Otology and Neurotology and the Politzer Society 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450088/
https://www.ncbi.nlm.nih.gov/pubmed/35418358
http://dx.doi.org/10.5152/iao.2022.21170

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9450088/
https://www.ncbi.nlm.nih.gov/pubmed/35418358
http://dx.doi.org/10.5152/iao.2022.21170

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