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Showing 1 to 1 of 1 for “"LCHAD"”.
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Molekulargenetische Untersuchungen im Kandidatengen HADHA bei Patientinnen mit HELLP-Syndrom und deren Kindern
… association of maternal HELLP syndrome and fetal LCHAD deficiency as a special inborn error of beta-oxidation of fatty acids, the responsible genes for LCHAD deficiency called HADHA and HADHB demanded attention. Especially the frequent G1528C mutation of HADHA was found in many fetal genotypes in …