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Four of the Most Common Mutations in Primary Hyperoxaluria Type 1 Unmask the Cryptic Mitochondrial Targeting Sequence of Alanine:glyoxylate Aminotransferase Encoded by the Polymorphic Minor Allele

Fargue, S; Lewin, J; Rumsby, G; Danpure, CJ; (2013) Four of the Most Common Mutations in Primary Hyperoxaluria Type 1 Unmask the Cryptic Mitochondrial Targeting Sequence of Alanine:glyoxylate Aminotransferase Encoded by the Polymorphic Minor Allele. JOURNAL OF BIOLOGICAL CHEMISTRY , 288 (4) pp. 2475-2484. 10.1074/jbc.M112.432617.

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Type: Article
Title: Four of the Most Common Mutations in Primary Hyperoxaluria Type 1 Unmask the Cryptic Mitochondrial Targeting Sequence of Alanine:glyoxylate Aminotransferase Encoded by the Polymorphic Minor Allele
DOI: 10.1074/jbc.M112.432617
Keywords: Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, ALANINE-GLYOXYLATE AMINOTRANSFERASE, ENZYME TRAFFICKING DEFECT, ALANINEGLYOXYLATE AMINOTRANSFERASE, SACCHAROMYCES-CEREVISIAE, PEROXISOMAL ALANINE, IMPORT, PHENOTYPE, DIMERIZATION, GENOTYPE, DISEASE
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/1380596
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