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

  1. Lookup NU author(s)
  2. Dr Kyle Thompson
  3. Frances White
  4. Steven Hardy
  5. Professor Robert Taylor
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
JournalJAMA Neurology
Year2018
Volume75
Issue1
Pages105-113
ISSN (print)2168-6149
ISSN (electronic)2168-6157
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
PublisherAmerican Medical Association
URLhttps://doi.org/10.1001/jamaneurol.2017.2065
DOI10.1001/jamaneurol.2017.2065
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