Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low
- 1 August 2000
- journal article
- Published by Springer Nature in Pediatric Research
- Vol. 48 (2) , 151-154
- https://doi.org/10.1203/00006450-200008000-00006
Abstract
No abstract availableKeywords
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