|
|||||
|
|
Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT |
|
| Authors: | Cassereau J Casasnovas C Gueguen N Malinge M-C Guillet V Reynier P Bonneau D Amati-Bonneau P Banchs I Volpini V Procaccio V Chevrollier A |
| Affiliation: | Biochemistry and Genetics Laboratory, National Centre for Neurodegenerative and Mitochondrial diseases, CHU Angers, 4 rue Larrey, Angers, France. |
| Abstract: | |
| Keywords: | |
| 本文献已被 PubMed 等数据库收录！ | |