Report for Kluijtmans LA

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References (3)

Title : Leucine Loading Test is Only Discriminative for 3-Methylglutaconic Aciduria Due to AUH Defect - Wortmann_2014_JIMD.Rep_16_1
Author(s) : Wortmann SB , Kluijtmans LA , Sequeira S , Wevers RA , Morava E
Ref : JIMD Rep , 16 :1 , 2014
Abstract : Wortmann_2014_JIMD.Rep_16_1
ESTHER : Wortmann_2014_JIMD.Rep_16_1
PubMedSearch : Wortmann_2014_JIMD.Rep_16_1
PubMedID: 24757000

Title : Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness - Wortmann_2012_Nat.Genet_44_797
Author(s) : Wortmann SB , Vaz FM , Gardeitchik T , Vissers LE , Renkema GH , Schuurs-Hoeijmakers JH , Kulik W , Lammens M , Christin C , Kluijtmans LA , Rodenburg RJ , Nijtmans LG , Grunewald A , Klein C , Gerhold JM , Kozicz T , van Hasselt PM , Harakalova M , Kloosterman W , Baric I , Pronicka E , Ucar SK , Naess K , Singhal KK , Krumina Z , Gilissen C , van Bokhoven H , Veltman JA , Smeitink JA , Lefeber DJ , Spelbrink JN , Wevers RA , Morava E , de Brouwer AP
Ref : Nat Genet , 44 :797 , 2012
Abstract : Wortmann_2012_Nat.Genet_44_797
ESTHER : Wortmann_2012_Nat.Genet_44_797
PubMedSearch : Wortmann_2012_Nat.Genet_44_797
PubMedID: 22683713
Gene_locus related to this paper: human-SERAC1

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