Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency : Clinical course and description of causal mutations in two patients von BOUCHARD, Luigi, ROBERT, Marie-France, BOUKAFTANE, Youssef, ASHMARINA, Lyudmila, SHUPEI WANG, MIZIORKO, Henry, MITCHELL, Grant A, VINAROV, Dmitriy, STANLEY, Charles A, THOMPSON, Geoffrey N, MORRIS, Andrew, LEONARD, James V, QUANT, Patti, HSU, Betty Y. L, BONEH, Avihu

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Cloning and characterization of the human mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase gene von Boukaftane, Youssef, Mitchell, Grant A

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Human Mitochondrial HMG CoA Synthase: Liver cDNA and Partial Genomic Cloning, Chromosome Mapping to 1p12-p13, and Possible Role in Vertebrate Evolution von Boukaftane, Youssef, Duncan, Alessandra, Wang, Shupei, Labuda, Damian, Robert, Marie-France, Sarrazin, Julie, Schappert, Keith, Mitchell, Grant A.

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