LPIN1 gene mutations: A major cause of severe rhabdomyolysis in early childhood [abstract] (2010)

Author(s): Michot C, Hubert L, Brivet M, De Meirleir L, Valayannopoulos V, Muller-Felber W, Venkateswaran R, Ogier H, Desguerre I, Altuzarra C, Thompson E, Smitka M, Huebner A, Husson M, Horvath R, Chinnery P, Vaz FM, Munnich A, Elpeleg O, Delahodde A, De Keyzer Y, De Lonlay P

    • Type of Article: Meeting Abstract
    • Date: 01-08-2010
    • Journal: Journal of Inherited Metabolic Disease
    • Volume: 33
    • Issue: s1
    • Pages: S56
    • Publisher: Springer
    • Publication type: Article
    • Bibliographic status: Published
    • ISSN (electronic): 1573-2665