HMG CoA Lyase Deficiency: Identification of Five Causal Point Mutations in Codons 41 and 42, Including a Frequent Saudi Arabian Mutation, R41Q
- 1 February 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (2) , 295-300
- https://doi.org/10.1086/301730
Abstract
No abstract availableKeywords
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