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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Dades bibliogràfiques
Publicat a:PLoS Genet
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2018
Matèries:
Research Article
Accés en línia: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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