Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy

CHN is genetically heterogeneous and its genetic basis is difficult to determine on features alone. CNTNAP1 encodes CASPR, integral in the paranodal junction high molecular mass complex. Nineteen individuals with biallelic variants have been described in association with severe congenital hypomyelin...

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Detalles Bibliográficos
Publicado en:Eur J Hum Genet
Main Authors: Low, KJ, Stals, K, Caswell, R, Wakeling, M, Clayton-Smith, J, Donaldson, A, Foulds, N, Norman, A, Splitt, M, Urankar, K, Vijayakumar, K, Majumdar, A, Study, DDD, Ellard, S, Smithson, SF
Formato: Artigo
Idioma:Inglês
Publicado: Springer International Publishing 2018
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5974240/
https://ncbi.nlm.nih.gov/pubmed/29511323
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-018-0110-x
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