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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
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