CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy

Ann Neurol. 2015 Nov;78(5):831. doi: 10.1002/ana.24464. Epub 2015 Aug 31.

Godelieve Morel¹, Cécile Rouzier^{1

2}, Annabelle Chaussenot^{1

2}, Samira Ait-El-Mkadem^{1

2}, Sylvie Bannwarth^{1

2}, Emmanuelle C Genin², Gaëlle Augé^{1

2}, Brigitte Chabrol³, Jean Pouget⁴, Marie Hélène Soriani⁵, Sabrina Sacconi⁵, Véronique Paquis-Flucklinger^{1

2}

¹ Department of Medical Genetics, National Center for Mitochondrial Diseases, Nice Teaching Hospital, Nice, France.
² IRCAN, UMR CNRS 7284/INSERM U1081/UNS, School of Medicine, Nice Sophia-Antipolis University, Nice, France.
³ Department of Neuropediatrics, Timone Hospital, Marseille Teaching Hospital, Marseille, France.
⁴ Department of Neurology, Timone Hospital, Marseille Teaching Hospital, Marseille, France.
⁵ National Center for Neuromuscular Disorders, Nice Teaching Hospital, Nice, France.

No abstract available

Publication types