ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment

Hearing impairment (HI) is a common disorder of sensorineural function with a highly heterogeneous genetic background. Although substantial progress has been made in the understanding of the genetic etiology of hereditary HI, many genes implicated in HI remain undiscovered. Via exome and Sanger sequ...

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Detalles Bibliográficos
Autores principales: Bharadwaj, Thashi, Schrauwen, Isabelle, Rehman, Sakina, Liaqat, Khurram, Acharya, Anushree, Giese, Arnaud P. J., Nouel-Saied, Liz M., Nasir, Abdul, Everard, Jenna L., Pollock, Lana M., Zhu, Shaoyuan, Bamshad, Michael J., Nickerson, Deborah A., Ali, Raja Hussain, Ullah, Asmat, Wali, Abdul, Ali, Ghazanfar, Santos-Cortez, Regie Lyn P., Ahmed, Zubair M., McDermott, Brian M., Ansar, Muhammad, Riazuddin, Saima, Ahmad, Wasim, Leal, Suzanne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738740/
https://www.ncbi.nlm.nih.gov/pubmed/34135477
http://dx.doi.org/10.1038/s41431-021-00913-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738740/
https://www.ncbi.nlm.nih.gov/pubmed/34135477
http://dx.doi.org/10.1038/s41431-021-00913-x

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