Authors: MITCHELL GA OZAND PT ROBERT MF ASHMARINA L ROBERTS J GIBSON KM WANDERS RJ WANG SP CHEVALIER I PLOCHL E MIZIORKO H

Citation: Ga. Mitchell et al., HMG COA LYASE DEFICIENCY - IDENTIFICATION OF 5 CAUSAL POINT MUTATIONSIN CODON-41 AND CODON-42, INCLUDING A FREQUENT SAUDI-ARABIAN MUTATION, R41Q, American journal of human genetics, 62(2), 1998, pp. 295-300