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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Detalhes bibliográficos
Publicado no:PLoS Genet
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2018
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6089448/
https://ncbi.nlm.nih.gov/pubmed/30067756
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1007550
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