Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults
- Resource Type
- Journal
- Authors
- Charif, Majida; Nasca, Alessia; Thompson, Kyle; Gerber, Sylvie; Makowski, Christine; Mazaheri, Neda; Bris, Celine; Goudenege, David; Legati, Andrea; Maroofian, Reza; Shariati, Gholamreza; Lamantea, Eleonora; Hopton, Sila; Ardissone, Anna; Moroni, Isabella; Giannotta, Melania; Siegel, Corinna; Strom, Tim M.; Prokisch, Holger; Vignal-Clermont, Catherine; Derrien, Sabine; Zanlonghi, Xavier; Kaplan, Josseline; Hamel, Christian P.; Leruez, Stephanie; Procaccio, Vincent; Bonneau, Dominique; Reynier, Pascal; White, Frances E.; Hardy, Steven A.; Barbosa, Ines A.; Simpson, Michael A.; Vara, Roshni; Trujillo, Yaumara Perdomo; Galehdari, Hamind; Deshpande, Charu; Haack, Tobias B.; Rozet, Jean-Michel; Taylor, Robert W.; Ghezzi, Daniele; Amati-Bonneau, Patrizia; Lenaers, Guy
- Source
- JAMA NEUROLOGY; JAN 2018, 75 1, p105-p113, 9p.
- Subject
- Language
- English
- ISSN
- 21686157