Authors:
Den Boer, MEJ
Ijlst, L
Wijburg, FA
Oostheim, W
Van Werkhoven, MA
Van Pampus, MG
Heymans, HSA
Wanders, RJA
Citation: Mej. Den Boer et al., 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, PEDIAT RES, 48(2), 2000, pp. 151-154