 |
Journal articles
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
Cited literature [6 references]
https://hal-riip.archives-ouvertes.fr/pasteur-02056171
Contributor : AbdelHakim Ben Hassine Connect in order to contact the contributor
Submitted on : Monday, March 4, 2019 - 2:29:19 PM
Last modification on : Wednesday, October 28, 2020 - 9:52:05 AM
Long-term archiving on: : Wednesday, June 5, 2019 - 3:19:57 PM
Contributor : AbdelHakim Ben Hassine Connect in order to contact the contributor
Submitted on : Monday, March 4, 2019 - 2:29:19 PM
Last modification on : Wednesday, October 28, 2020 - 9:52:05 AM
Long-term archiving on: : Wednesday, June 5, 2019 - 3:19:57 PM
File
Mitochondrial Myopathy.pdf
Publication funded by an institution
Licence
Distributed under a Creative Commons Attribution - NonCommercial - NoDerivatives 4.0 International License