Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults

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Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults

Author: 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; Rozet, Jean-Michel; Taylor, Robert W.; Ghezzi, Daniele; Amati-Bonneau, Patrizia; Lenaers, Guy; Haack, Tobias
Tübinger Autor(en):
Haack, Tobias
Published in: Jama Neurology (2018), Bd. 75, H. 1, S. 105-113
Verlagsangabe: American Medical Association
Language: English
Full text: http://dx.doi.org/10.1001/jamaneurol.2017.2065
ISSN: 2168-6157
DDC Classifikation: 610 - Medicine and health
Dokumentart: Artikel
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