Primary hyperoxaluria type I due to a point mutation of T to C in the coding region of the serine:pyruvate aminotransferase gene
- 15 May 1991
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 176 (3) , 1093-1099
- https://doi.org/10.1016/0006-291x(91)90396-o
Abstract
No abstract availableKeywords
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