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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Bibliografiske detaljer
Udgivet i:Front Neurol
Main Authors: Biotteau, Maëlle, Déjean, Sébastien, Lelong, Sandrine, Iannuzzi, Stéphanie, Faure-Marie, Nathalie, Castelnau, Pierre, Rivier, François, Lauwers-Cancès, Valérie, Baudou, Eloïse, Chaix, Yves
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2020
Fag:
Neurology
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7214842/
https://ncbi.nlm.nih.gov/pubmed/32431664
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.00368
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