Progressive ataxia of Charolais cattle highlights a role of KIF1C in sustainable myelination

Hereditary spastic paraplegias (HSPs) are clinically and genetically heterogeneous human neurodegenerative diseases. Amongst the identified genetic causes, mutations in genes encoding motor proteins such as kinesins have been involved in various HSP clinical isoforms. Mutations in KIF1C are responsi...

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Detalles Bibliográficos
Autores principales: Duchesne, Amandine, Vaiman, Anne, Frah, Magali, Floriot, Sandrine, Legoueix-Rodriguez, Sabrina, Desmazières, Anne, Fritz, Sébastien, Beauvallet, Christian, Albaric, Olivier, Venot, Eric, Bertaud, Maud, Saintilan, Romain, Guatteo, Raphaël, Esquerré, Diane, Branchu, Julien, Fleming, Anaïs, Brice, Alexis, Darios, Frédéric, Vilotte, Jean-Luc, Stevanin, Giovanni, Boichard, Didier, El Hachimi, Khalid Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089448/
https://www.ncbi.nlm.nih.gov/pubmed/30067756
http://dx.doi.org/10.1371/journal.pgen.1007550

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089448/
https://www.ncbi.nlm.nih.gov/pubmed/30067756
http://dx.doi.org/10.1371/journal.pgen.1007550

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