Differential impacts of Cntnap2 heterozygosity and Cntnap2 null homozygosity on axon and myelinated fiber development in mouse

Over the last decade, a large variety of alterations of the Contactin Associated Protein 2 (CNTNAP2) gene, encoding Caspr2, have been identified in several neuronal disorders, including neurodevelopmental disorders and peripheral neuropathies. Some of these alterations are homozygous but most are he...

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Detalles Bibliográficos
Autores principales: Cifuentes-Diaz, Carmen, Canali, Giorgia, Garcia, Marta, Druart, Mélanie, Manett, Taylor, Savariradjane, Mythili, Guillaume, Camille, Le Magueresse, Corentin, Goutebroze, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9922869/
https://www.ncbi.nlm.nih.gov/pubmed/36793543
http://dx.doi.org/10.3389/fnins.2023.1100121

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