Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/63835
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Type: Journal article
Title: LPIN1 gene mutations: A major cause of severe rhabdomyolysis in early childhood
Author: 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, F.
Munnich, A.
Elpeleg, O.
Delahodde, A.
et al.
Citation: Human Mutation, 2010; 31(7):E1564-E1573
Publisher: Wiley-Liss
Issue Date: 2010
ISSN: 1059-7794
Statement of
Responsibility: 
Caroline Michot... Elizabeth Thompson... et al.
Keywords: Rhabdomyolysis; LPIN1; intragenic deletion; founder effect.
Rights: © 2010 Wiley-Liss, Inc.
RMID: 0020100411
DOI: 10.1002/humu.21282
Appears in Collections:Paediatrics publications

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