methylglutaconyl-CoA hydratase, mitochondrial isoform X11 [Homo sapien - Protein

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Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. [J Inherit Metab Dis. 2013]
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature.
Wortmann SB, Duran M, Anikster Y, Barth PG, Sperl W, Zschocke J, Morava E, Wevers RA. J Inherit Metab Dis. 2013 Nov; 36(6):923-8. Epub 2013 Jan 8.
Phenotypic heterogeneity in two siblings with 3-methylglutaconic aciduria type I caused by a novel intragenic deletion. [Mol Genet Metab. 2011]
Phenotypic heterogeneity in two siblings with 3-methylglutaconic aciduria type I caused by a novel intragenic deletion.
Mercimek-Mahmutoglu S, Tucker T, Casey B. Mol Genet Metab. 2011 Nov; 104(3):410-3. Epub 2011 Jul 26.
3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy. [Neurology. 2010]
3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy.
Wortmann SB, Kremer BH, Graham A, Willemsen MA, Loupatty FJ, Hogg SL, Engelke UF, Kluijtmans LA, Wanders RJ, Illsinger S, et al. Neurology. 2010 Sep 21; 75(12):1079-83.

RefSeq genomic sequence
See the genomic reference sequence for the AUH gene (NG_008017.1).
RefSeq mRNA
See reference mRNA sequence for the AUH gene (XM_054363162.1).
RefSeq protein isoforms
See 33 reference sequence protein isoforms for the AUH gene.

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