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MCCC1 encodes the large subunit of 3-methylcrotonyl-CoA carboxylase. De plus, nous expédions Methylcrotonoyl-CoA Carboxylase 1 (Alpha) Anticorps (36) et Methylcrotonoyl-CoA Carboxylase 1 (Alpha) Protéines (7) et beaucoup plus de produits pour cette protéine.
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This study reports data mainly obtained from the Portuguese newborn screening program collected over a ten-year period. Analysis of the MCCC1 and MCCC2 (Montrer MCCC2 Kits ELISA) genes yielded 26 previously unreported mutations and a variant of clinically unknown significance.
Our study provides strong support for the susceptibility role of RAB7L1/NUCKS1 rs823118 and MCCC1 rs12637471 in sporadic Parkinson's disease in a Han Chinese population
Novel mutations in MCCC1 gene were identified in Chinese population. The expression profiles of two splice mutations (c.639+2T>A and c.639+5G>T) were also characterized.
Four new point mutations were detected in the MCCC1 gene in patients with maternal 3-methylcrotonyl coenzyme deficiency.
This study demonistrated that Mainland China demonstrates that MCCC1/LAMP3 (Montrer CD63 Kits ELISA) (rs11711441) is associated with a lower risk of Parkinson's disease.
3-methylcrotonyl-CoA carboxylase (Montrer MCCC2 Kits ELISA) inhibition has a role in increased excretion of 3-hydroxyisovaleric acid in valproate-treated patients
Mutation in 3-methylcrotonyl CoA carboxylase 1 gene is associated with 3-methylcrotonyl-CoA carboxylase (Montrer MCCC2 Kits ELISA) deficiency.
study reports eight different mutant alleles of MCCC1 or MCCC2 including six novel mutations in Korean patients with 3-methylcrotonyl-CoA carboxylase (MCC) deficiency
identified two novel MCCA and four novel MCCB mutant alleles from five MCC-deficient patients
factors other than the genotype at the MCCA and MCCB loci have a major influence on the phenotype of MCC deficiency
Studies indicate that mutations in either 3-methylcrotonyl CoA carboxylase (Montrer MCCC2 Kits ELISA) MCCA (At1g03090) or MCCB (Montrer MCCC2 Kits ELISA) (At4g34030) block mitochondrial Leu catabolism, as inferred from the increased accumulation of Leu.
This gene encodes the large subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism.
3-methylcrotonyl-CoA carboxylase 1
, 3-methylcrotonyl-CoA carboxylase biotin-containing subunit
, 3-methylcrotonyl-CoA:carbon dioxide ligase subunit alpha
, MCCase subunit alpha
, methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial
, methylcrotonoyl-Coenzyme A carboxylase 1 (alpha)