First characterization of LHON pedigrees in North Africa
Eye (Lond)
.
2020 Nov;34(11):2138-2139.
doi: 10.1038/s41433-019-0755-x.
Epub 2020 Jan 2.
Authors
Aymane Bouzidi
1
2
3
,
Nisrine Aboussair
4
5
,
Majida Charif
1
6
,
Ghita Amalou
1
2
3
,
David Goudenège
1
7
,
Valérie Desquiret-Dumas
1
7
,
Céline Bris
1
7
,
Najat Sifeddine
2
,
Halima Nahili
2
,
Meriem Elqabli
4
,
Kenza Dafir
4
5
,
Mostafa Kandil
3
,
Patrizia Amati-Bonneau
1
7
,
Vincent Procaccio
1
7
,
Abdelhamid Barakat
2
,
Guy Lenaers
8
Affiliations
1
MitoLab team, Institut MitoVasc, UMR CNRS 6015, INSERM U1083, Université d'Angers, Angers, France.
2
Human Molecular Genetics Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco.
3
Team of Anthropogenetics and Biotechnologies, Faculty of Sciences, Chouaib Doukkali University, Eljadida, Morocco.
4
Genetic Department, Clinical Research Center, Mohammed VI University Hospital Center, Marrakech, Morocco.
5
Faculty of Medicine and Pharmacy, Cadi Ayyad University, Marrakech, Morocco.
6
Laboratory of Physiology, Genetics and Ethnopharmacology, Faculty of Sciences, University Mohammed Premier, Oujda, Morocco.
7
Département de Biochimie et Génétique, CHU d'Angers, Angers, France.
8
MitoLab team, Institut MitoVasc, UMR CNRS 6015, INSERM U1083, Université d'Angers, Angers, France. guy.lenaers@inserm.fr.
PMID:
31896800
PMCID:
PMC7784990
DOI:
10.1038/s41433-019-0755-x
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
MeSH terms
Africa, Northern
DNA, Mitochondrial*
Humans
Mutation
Optic Atrophy, Hereditary, Leber*
Pedigree
Substances
DNA, Mitochondrial