Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse-Reference-Cited by-同舟云学术

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse

Published:2019-03-14 Issue:1 Volume:138 Page:123-145
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Genin Emmanuelle C.,Madji Hounoum Blandine,Bannwarth Sylvie,Fragaki Konstantina,Lacas-Gervais Sandra,Mauri-Crouzet Alessandra,Lespinasse Françoise,Neveu Julien,Ropert Baptiste,Augé Gaelle,Cochaud Charlotte,Lefebvre-Omar Cynthia,Bigou Stéphanie,Chiot Aude,Mochel Fanny,Boillée Séverine,Lobsiger Christian S.,Bohl Delphine,Ricci Jean-Ehrland,Paquis-Flucklinger Véronique

Funder

Agence Nationale de la Recherche

AFM-Téléthon

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-019-01988-z.pdf

Reference46 articles.

1. Auranen M, Ylikallio E, Shcherbii M, Paetau A, Kiuru-Enari S, Toppila JP et al (2015) CHCHD10 variant p.(Gly66Val) causes axonal Charcot–Marie–Tooth disease. Neurol Genet 1:e1. https://doi.org/10.1212/nxg.0000000000000003

2. Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K et al (2014) A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement. Brain J Neurol 137:2329–2345. https://doi.org/10.1093/brain/awu138