Cargando…
Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations
In the present study, genotype–phenotype correlations in eight Dutch DFNB8/10 families with compound heterozygous mutations in TMPRSS3 were addressed. We compared the phenotypes of the families by focusing on the mutation data. The compound heterozygous variants in the TMPRSS3 gene in the present fa...
Autores principales: | Weegerink, Nicole J. D., Schraders, Margit, Oostrik, Jaap, Huygen, Patrick L. M., Strom, Tim M., Granneman, Susanne, Pennings, Ronald J. E., Venselaar, Hanka, Hoefsloot, Lies H., Elting, Mariet, Cremers, Cor W. R. J., Admiraal, Ronald J. C., Kremer, Hannie, Kunst, Henricus P. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214237/ https://www.ncbi.nlm.nih.gov/pubmed/21786053 http://dx.doi.org/10.1007/s10162-011-0282-3 |
Ejemplares similares
-
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin
por: Aller, Elena, et al.
Publicado: (2010) -
Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction
por: Wesdorp, Mieke, et al.
Publicado: (2018) -
Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1
por: Hogewind, Barend F.T., et al.
Publicado: (2010) -
EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus
por: Hoefsloot, Lies H, et al.
Publicado: (2013) -
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
por: Smits, Jeroen J., et al.
Publicado: (2018)