succinate--hydroxymethylglutarate CoA-transferase isoform 3 [Homo sapi - Protein

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Genetic mapping of glutaric aciduria, type 3, to chromosome 7 and identification of mutations in c7orf10. [Am J Hum Genet. 2008]
Genetic mapping of glutaric aciduria, type 3, to chromosome 7 and identification of mutations in c7orf10.
Sherman EA, Strauss KA, Tortorelli S, Bennett MJ, Knerr I, Morton DH, Puffenberger EG. Am J Hum Genet. 2008 Nov; 83(5):604-9.
Glutaric aciduria type III: a distinctive non-disease? [J Inherit Metab Dis. 2002]
Glutaric aciduria type III: a distinctive non-disease?
Knerr I, Zschocke J, Trautmann U, Dorland L, de Koning TJ, Müller P, Christensen E, Trefz FK, Wündisch GF, Rascher W, et al. J Inherit Metab Dis. 2002 Oct; 25(6):483-90.
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder. [J Inherit Metab Dis. 1991]
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.
Bennett MJ, Pollitt RJ, Goodman SI, Hale DE, Vamecq J. J Inherit Metab Dis. 1991; 14(2):165-73.

RefSeq genomic sequence
See the genomic reference sequence for the SUGCT gene (NG_023422.3).
RefSeq mRNA
See reference mRNA sequence for the SUGCT gene (NM_001193313.2).

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NP_001180242 [Domain Mapping of Disease Mut...]
NP_001180242
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
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succinate--hydroxymethylglutarate CoA-transferase isoform 3 [Homo sapiens]
succinate--hydroxymethylglutarate CoA-transferase isoform 3 [Homo sapiens]
gi|1769843778|ref|NP_001180242.2|

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