Fundamental Properties of Aldehyde Dehydrogenase 2 (ALDH2) and the Importance of the ALDH2 Polymorphism
Author:
Affiliation:
1. Department of Social Medicine, Saga University School of Medicine
Publisher
Japanese Society for Hygiene
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjh/71/1/71_55/_pdf
Reference178 articles.
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2. (2) Jackson B, Brocker C, Thompson DC, Black W, Vasiliou K, Nebert DW, et al. Update on the aldehyde dehydrogenase gene (ALDH) superfamily. Hum Genomics 2011;5:283–303.
3. (3) Dupe V, Matt N, Garnier JM, Chambon P, Mark M, Ghyselinck NB. A newborn lethal defect due to inactivation of retinaldehyde dehydrogenase type 3 is prevented by maternal retinoic acid treatment. Proc Natl Acad Sci USA 2003;100:14036–14041.
4. (4) Niederreither K, Subbarayan V, Dolle P, Chambon P. Embryonic retinoic acid synthesis is essential for early mouse post-implantation development. Nat Genet 1999;21:444–448.
5. (5) Gibson KM, Sweetman L, Kozich V, Pijackova A, Tscharre A, Cortez A, et al. Unusual enzyme findings in five patients with metabolic profiles suggestive of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria). J Inherit Metab Dis 1998;21:255–261.
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