Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

Congenital hearing impairment (HI) is genetically heterogeneous making its genetic diagnosis challenging. Investigation of novel HI genes and variants will enhance our understanding of the molecular mechanisms and to aid genetic diagnosis. We performed exome sequencing and analysis using DNA samples...

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Detalles Bibliográficos
Autores principales: Adadey, Samuel M., Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Bharadwaj, Thashi, Esoh, Kevin K., Basit, Sulman, Acharya, Anushree, Nouel-Saied, Liz M., Liaqat, Khurram, Wonkam-Tingang, Edmond, Mowla, Shaheen, Awandare, Gordon A., Ahmad, Wasim, Leal, Suzanne M., Wonkam, Ambroise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612923/
https://www.ncbi.nlm.nih.gov/pubmed/34226616
http://dx.doi.org/10.1038/s10038-021-00954-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8612923/
https://www.ncbi.nlm.nih.gov/pubmed/34226616
http://dx.doi.org/10.1038/s10038-021-00954-6

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