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"3-hydroxy-3-methylglutaryl-coa"
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (also known as HMG-CoA lyase deficiency) is an uncommon inherited disorder in which ... not show signs and symptoms of the condition. 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency 3-OH 3-CH3 glutaric aciduria ...
- ... Health Condition 3-hydroxy-3-methylglutarate-CoA lyase 3-hydroxy-3-methylglutaryl-Coenzyme A lyase 3-hydroxymethyl-3-methylglutaryl-CoA lyase 3- ... CoA lyase HMGCL_HUMAN Tests of HMGCL PubMed 3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE; HMGCL NCBI Gene ClinVar Al-Sayed M, ...
- ... called 3-methylglutaconyl-CoA into another molecule called 3-hydroxy-3-methylglutaryl-CoA.3-methylglutaconyl-CoA hydratase also has the ability ...