HSP and deafness: Neurocristopathy caused by a novel mosaic SOX10 mutation

OBJECTIVE: To identify the underlying genetic cause in 2 sisters affected with progressive lower extremity spasticity, neuropathy, and early-onset deafness. METHODS: Whole-exome sequencing was performed, and segregation testing of variants was investigated using targeted Sanger sequencing. An inheri...

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Detalles Bibliográficos
Autores principales: Donkervoort, Sandra, Bharucha-Goebel, Diana, Yun, Pomi, Hu, Ying, Mohassel, Payam, Hoke, Ahmet, Zein, Wadih M., Ezzo, Daniel, Atherton, Andrea M., Modrcin, Ann C., Dasouki, Majed, Foley, A. Reghan, Bönnemann, Carsten G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432370/
https://www.ncbi.nlm.nih.gov/pubmed/28534044
http://dx.doi.org/10.1212/NXG.0000000000000151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5432370/
https://www.ncbi.nlm.nih.gov/pubmed/28534044
http://dx.doi.org/10.1212/NXG.0000000000000151

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