Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy
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, SFLangue:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/s41431-018-0110-x
Date:
March, 2018
Fichier:
PDF, 2.25 MB
english, 2018
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