An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1
- 1 August 1991
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 87 (4) , 394-396
- https://doi.org/10.1007/bf00197154
Abstract
No abstract availableKeywords
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- Human peroxisomal l-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codonBiochemical Journal, 1990
- Domain characterization of rabbit skeletal muscle myosin light chain kinase.Journal of Biological Chemistry, 1990
- Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type IFEBS Letters, 1986