Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population

Otosclerosis is a common form of hearing loss which typically presents in young adults. The disease has a familial, monogenic form and a non-familial form with a more complex aetiology. A previous genome wide association study identified evidence that variants within RELN are associated with the con...

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Detalles Bibliográficos
Autores principales: Mowat, Andrew J., Crompton, Michael, Ziff, Joanna L., Aldren, Christopher P., Lavy, Jeremy A., Saeed, Shakeel R., Dawson, Sally J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973954/
https://www.ncbi.nlm.nih.gov/pubmed/29728750
http://dx.doi.org/10.1007/s00439-018-1889-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973954/
https://www.ncbi.nlm.nih.gov/pubmed/29728750
http://dx.doi.org/10.1007/s00439-018-1889-9

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