Title : Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylation - Wortmann_2006_Mol.Genet.Metab_88_47 |
Author(s) : Wortmann S , Rodenburg RJ , Huizing M , Loupatty FJ , de Koning T , Kluijtmans LA , Engelke U , Wevers R , Smeitink JA , Morava E |
Ref : Mol Genet Metab , 88 :47 , 2006 |
Abstract : Wortmann_2006_Mol.Genet.Metab_88_47 |
ESTHER : Wortmann_2006_Mol.Genet.Metab_88_47 |
PubMedSearch : Wortmann_2006_Mol.Genet.Metab_88_47 |
PubMedID: 16527507 |
Gene_locus related to this paper: human-SERAC1 |
Gene_locus related to this paper: human-SERAC1 |
Wortmann S, Rodenburg RJ, Huizing M, Loupatty FJ, de Koning T, Kluijtmans LA, Engelke U, Wevers R, Smeitink JA, Morava E (2006)
Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylation
Mol Genet Metab
88 :47
Wortmann S, Rodenburg RJ, Huizing M, Loupatty FJ, de Koning T, Kluijtmans LA, Engelke U, Wevers R, Smeitink JA, Morava E (2006)
Mol Genet Metab
88 :47