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

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Verfasser: Den Boer, Margarethe E J
Ijlst, Lodewijk
Wijburg, Frits A
Oostheim, Wendy
Van Werkhoven, Michiel A
Van Pampus, Marielle G
Heymans, Hugo S A
Wanders, Ronald J A
Dokumenttyp: Artikel
Erscheinungsdatum: 2000
Reihe/Periodikum: Pediatric Research ; volume 48, issue 2, page 151-154 ; ISSN 0031-3998 1530-0447
Verlag/Hrsg.: Springer Science and Business Media LLC
Sprache: unknown
Permalink: https://search.fid-benelux.de/Record/base-29050620
Datenquelle: BASE; Originalkatalog
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Link(s) : http://dx.doi.org/10.1203/00006450-200008000-00006