Sporadic and Familial Variants in NF1: An Explanation of the Wide Variability in Neurocognitive Phenotype?

Background: Cognitive impairment is the most common neurological manifestation in NF1 and occurs in 30–70% of NF1 cases. The onset and severity of each specific cognitive deficit varies greatly from child to child, with no apparent external causes. The wide variability of phenotype is the most compl...

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Detalles Bibliográficos
Autores principales: Biotteau, Maëlle, Déjean, Sébastien, Lelong, Sandrine, Iannuzzi, Stéphanie, Faure-Marie, Nathalie, Castelnau, Pierre, Rivier, François, Lauwers-Cancès, Valérie, Baudou, Eloïse, Chaix, Yves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214842/
https://www.ncbi.nlm.nih.gov/pubmed/32431664
http://dx.doi.org/10.3389/fneur.2020.00368

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214842/
https://www.ncbi.nlm.nih.gov/pubmed/32431664
http://dx.doi.org/10.3389/fneur.2020.00368

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