Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India

BACKGROUND & OBJECTIVES: Hearing impairment is a common and heterogeneous sensory disorder in humans. Among about 90 genes, which are known to be associated with hearing impairment, mutations in the GJB2 (gap junction protein beta 2) gene are the most prevalent in individuals with hereditary hea...

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Detalles Bibliográficos
Autores principales: Singh, Pawan Kumar, Ghosh, Manju, Sharma, Shipra, Shastri, Shivaram, Gupta, Neerja, Chowdhury, Madhumita Roy, Anand, Anuranjan, Kabra, Madhulika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663163/
https://www.ncbi.nlm.nih.gov/pubmed/28862181
http://dx.doi.org/10.4103/ijmr.IJMR_397_15

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663163/
https://www.ncbi.nlm.nih.gov/pubmed/28862181
http://dx.doi.org/10.4103/ijmr.IJMR_397_15

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