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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.
Genomics. 1994 Oct;23(3):552-9. doi: 10.1006/geno.1994.1542.
Genomics. 1994.
PMID: 7851882
Cloning and characterization of the human mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase gene.
Boukaftane Y, Mitchell GA.
Boukaftane Y, et al.
Gene. 1997 Aug 22;195(2):121-6. doi: 10.1016/s0378-1119(97)00067-x.
Gene. 1997.
PMID: 9305755
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Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients.
Bouchard L, Robert MF, Vinarov D, Stanley CA, Thompson GN, Morris A, Leonard JV, Quant P, Hsu BY, Boneh A, Boukaftane Y, Ashmarina L, Wang S, Miziorko H, Mitchell GA.
Bouchard L, et al. Among authors: boukaftane y.
Pediatr Res. 2001 Mar;49(3):326-31. doi: 10.1203/00006450-200103000-00005.
Pediatr Res. 2001.
PMID: 11228257
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Medical aspects of ketone body metabolism.
Mitchell GA, Kassovska-Bratinova S, Boukaftane Y, Robert MF, Wang SP, Ashmarina L, Lambert M, Lapierre P, Potier E.
Mitchell GA, et al. Among authors: boukaftane y.
Clin Invest Med. 1995 Jun;18(3):193-216.
Clin Invest Med. 1995.
PMID: 7554586
Review.
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Inborn errors of ketogenesis.
Mitchell GA, Wang SP, Ashmarina L, Robert MF, Bouchard G, Laurin N, Kassovska-Bratinova S, Boukaftane Y.
Mitchell GA, et al. Among authors: boukaftane y.
Biochem Soc Trans. 1998 May;26(2):136-40. doi: 10.1042/bst0260136.
Biochem Soc Trans. 1998.
PMID: 9649735
Review.
No abstract available.
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Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis.
Boukaftane Y, Khoris J, Moulard B, Salachas F, Meininger V, Malafosse A, Camu W, Rouleau GA.
Boukaftane Y, et al.
Can J Neurol Sci. 1998 Aug;25(3):192-6. doi: 10.1017/s0317167100034004.
Can J Neurol Sci. 1998.
PMID: 9706719
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