CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis

OBJECTIVE: To explore the phenotypic spectrum and pathophysiology of human disease deriving from mutations in the CNTNAP1 gene. METHODS: In a field study on consanguineous Palestinian families, we identified 3 patients carrying homozygous mutations in the CNTNAP1 gene using whole-exome sequencing. A...

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Detalles Bibliográficos
Autores principales: Hengel, Holger, Magee, Alex, Mahanjah, Muhammad, Vallat, Jean-Michel, Ouvrier, Robert, Abu-Rashid, Mohammad, Mahamid, Jamal, Schüle, Rebecca, Schulze, Martin, Krägeloh-Mann, Ingeborg, Bauer, Peter, Züchner, Stephan, Sharkia, Rajech, Schöls, Ludger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363873/
https://www.ncbi.nlm.nih.gov/pubmed/28374019
http://dx.doi.org/10.1212/NXG.0000000000000144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363873/
https://www.ncbi.nlm.nih.gov/pubmed/28374019
http://dx.doi.org/10.1212/NXG.0000000000000144

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