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Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1

Fargue, S; Rumsby, G; Danpure, CJ; (2013) Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE , 1832 (10) pp. 1776-1783. 10.1016/j.bbadis.2013.04.010.

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Type: Article
Title: Multiple mechanisms of action of pyridoxine in primary hyperoxaluria type 1
DOI: 10.1016/j.bbadis.2013.04.010
Keywords: Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Biophysics, Cell Biology, Primary hyperoxaluria, Alanine:glyoxylate aminotransferase, Hereditary metabolic disease, Kidney stone, Pyridoxine, Vitamin B6, ALANINE-GLYOXYLATE AMINOTRANSFERASE, LINKED SIDEROBLASTIC ANEMIA, ENZYME TRAFFICKING DEFECT, I PRIMARY HYPEROXALURIA, GYRATE ATROPHY, ALANINE/GLYOXYLATE AMINOTRANSFERASE, VITAMIN-B6 METABOLISM, PEROXISOMAL ALANINE, TARGETING SEQUENCE, MUTATION
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences
URI: http://discovery.ucl.ac.uk/id/eprint/1450304
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