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Neurologic phenotypes associated with mutations in RTN4IP1 (OPA10) in children and young adults

Lookup NU author(s): Dr Kyle Thompson, Frances White, Steven Hardy, Professor Robert Taylor

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Author(s): Charif M, Nasca A, Thompson K, Gerber S, Makowski C, Mazaheri N, Bris C, Goudenege D, Legati A, Maroofian R, Shariati G, Lamantea E, Hopton S, Ardissone A, Moroni I, Giannotta M, Siegel C, Strom TM, Prokisch H, Vignal-Clermont C, Derrien S, Zanlonghi X, Kaplan J, Hamel CP, Leruez S, Procaccio V, Bonneau D, Reynier P, White FE, Hardy SA, Barbosa IA, Simpson MA, Vara R, Trujillo YP, Galehdari H, Deshpande C, Haack TB, Rozet J-M, Taylor RW, Ghezzi D, Amati-Bonneau P, Lenaers G

Publication type: Article

Journal: JAMA Neurology

Year: 2018

Volume: 75

Issue: 1

Pages: 105-113

Online publication date: 27/11/2017

Acceptance date: 08/06/2017

Print publication date: 01/01/2018

ISSN (print): 2168-6149

ISSN (electronic): 2168-6157

Publisher: American Medical Association

URL: https://doi.org/10.1001/jamaneurol.2017.2065

DOI: 10.1001/jamaneurol.2017.2065


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