Case Report: Novel mutations in TBC1D24 are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disability

Mutations disrupting presynaptic protein TBC1D24 are associated with a variable neurological phenotype, including DOORS syndrome, myoclonic epilepsy, early-infantile epileptic encephalopathy, and non-syndromic hearing loss. In this report, we describe a family segregating autosomal dominant epilepsy...

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Detalles Bibliográficos
Autores principales: Banuelos, Erika, Ramsey, Keri, Belnap, Newell, Krishnan, Malavika, Balak, Chris, Szelinger, Szabolcs, Siniard, Ashley L., Russell, Megan, Richholt, Ryan, De Both, Matt, Piras, Ignazio, Naymik, Marcus, Claasen, Ana M., Rangasamy, Sampathkumar, Huentelman, Matthew J., Craig, David W., Campeau, Philippe M., Narayanan, Vinodh, Schrauwen, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473401/
https://www.ncbi.nlm.nih.gov/pubmed/28663785
http://dx.doi.org/10.12688/f1000research.10588.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473401/
https://www.ncbi.nlm.nih.gov/pubmed/28663785
http://dx.doi.org/10.12688/f1000research.10588.1

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