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

Autor: Raphaël Guatteo, Diane Esquerre, Sabrina Legoueix-Rodriguez, Maud Bertaud, Anaïs Fleming, Julien Branchu, Christian Beauvallet, Romain Saintilan, Alexis Brice, Amandine Duchesne, Anne Vaiman, Frédéric Darios, Anne Desmazières, Giovanni Stevanin, Sandrine Floriot, Magali Frah, Olivier Albaric, Eric Venot, Khalid Hamid El Hachimi, Sébastien Fritz, Jean-Luc Vilotte, Didier Boichard

Publikováno v: PLoS Genetics
PLoS Genetics, Public Library of Science, 2018, 14 (8), pp.1-25. ⟨10.1371/journal.pgen.1007550⟩
Plos Genetics 8 (14), 1-25. (2018)
PLoS Genetics, 2018, 14 (8), pp.1-25. ⟨10.1371/journal.pgen.1007550⟩
PLoS Genetics, Vol 14, Iss 8, p e1007550 (2018)

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422ecf5137fe6992d8957c0ab7e85fc4
https://hal.inrae.fr/hal-02624522