Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy

PURPOSE: To define the phenotype and elucidate the molecular basis for an autosomal recessively inherited optic atrophy and auditory neuropathy in a consanguineous family with two affected children. METHODS: Family members underwent detailed ophthalmologic, electrophysiological, and audiological ass...

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Detalles Bibliográficos
Autores principales: Meyer, Esther, Michaelides, Michel, Tee, Louise J., Robson, Anthony G., Rahman, Fatimah, Pasha, Shanaz, Luxon, Linda M., Moore, Anthony T., Maher, Eamonn R.
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855733/
https://www.ncbi.nlm.nih.gov/pubmed/20405026

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855733/
https://www.ncbi.nlm.nih.gov/pubmed/20405026

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