Molecular prenatal diagnosis of 3-hydroxy−3-methylglutaryl coa lyase deficiencyGrant A. Mitchell; Cornelis Jakobs; K. Michael Gebson; Marie-France Robert; Alberto Burlina; Carlo Dionisi-Vici; Louis Dallaire · 1995

Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi populationMoeenaldeen Al-Sayed; Faiqa Imtiaz; Osama A Alsmadi; Mohammed S Rashed; Brian F Meyer · 2006

Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl–CoA lyase deficiencyDr Huda Y. Zoghbi; J. Edward Spence; Arthur L. Beaudet; William E. O'Brien; Clay J. Goodman; Kenneth M. Gibson · 1986

Molecular analysis of Taiwanese patients with 3-Hydroxy-3-methylglutaryl CoA lyase deficiencyWei-De Lin; Chung-Hsing Wang; Chien-Chen Lai; Yushin Tsai; Jer-Yuarn Wu; Chih-Ping Chen; Fuu-Jen Tsai · 2009

Ketogenic flux from lipids and leucine, assessment in 3-hydroxy-3-methylglutaryl CoA lyase deficiencyHOLMES, Heather C.; BURNS, Shamus P.; CHALMERS, Ronald A.; BAIN, Murray S.; ILES, Richard A. · Biochemical Society Transactions · 1995

Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiencyJunko Muroi; Tohru Yorifuji; Ayumi Uematsu; Yosuke Shigematsu; Kazumichi Onigata; Hiroaki Maruyama; Tatsuro Nobutoki; Akiko Kitamura; Tatsutoshi Nakahata · 2000

92 LONG TERM USE OF D-HYDROXYBUTYRATE (DOHB) IN THE MANAGEMENT OF A PATIENT WITH 3-HYDROXY-3-METHYLGLUTARYL CoA (HMGCoA) LYASE DEFICIENCYFrançois, B; Bachmann, C · Pediatric Research · 1986

3-Hydroxy-3-Methylglutaryl CoA Lyase (HL): Mouse and Human HL Gene (HMGCL) Cloning and Detection of Large Gene Deletions in Two Unrelated HL-Deficient PatientsS.P. Wang; M-F. Robert; K.M. Gibson; R.J.A. Wanders; G.A. Mitchell · 1996