Identification of the α-Aminoadipic Semialdehyde Synthase Gene, Which Is Defective in Familial Hyperlysinemia
- 1 June 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 66 (6) , 1736-1743
- https://doi.org/10.1086/302919
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of ?complete ring? syndromeAmerican Journal of Medical Genetics, 1999
- RETRACTED: Detecting patterns of protein distribution and gene expression in silicoProceedings of the National Academy of Sciences, 1999
- Lysine-ketoglutarate reductase and saccharopine dehydrogenase from Arabidopsis thaliana: nucleotide sequence and characterization.Plant Molecular Biology, 1997
- Identification of peroxisomal targeting signals located at the carboxy terminus of four peroxisomal proteins.The Journal of cell biology, 1988
- α-Aminoadipate Pathway for the Biosynthesis of Lysine in Lower EukaryotesCRC Critical Reviews in Microbiology, 1985
- Orotate phosphoribosyltransferase and orotidylate decarboxylase from Crithidia luciliae: Subcellular location of the enzymes and a study of substrate channelingArchives of Biochemistry and Biophysics, 1984
- HYPERLYSINEMIA WITHOUT CLINICAL FINDINGSActa Paediatrica, 1981
- LYSINE METABOLISM IN THE RAT BRAIN: THE PIPECOLIC ACID‐FORMING PATHWAYJournal of Neurochemistry, 1978
- Familial hyperlysinemia with lysine-ketoglutarate reductase insufficiencyJournal of Clinical Investigation, 1969
- HyperlysinemiaArchives of Pediatrics & Adolescent Medicine, 1964