Global ETD Search
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Showing 1 to 1 of 1 for “"HADHA"”.
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Molekulargenetische Untersuchungen im Kandidatengen HADHA bei Patientinnen mit HELLP-Syndrom und deren Kindern
… 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 these cases of clinical association. HADHA and HADHB seemed to be candidate genes for HELLP syndrome. Based upon this we …