Author:
LEUMANN ERNST,HOPPE BERND
Publisher
American Society of Nephrology (ASN)
Subject
Nephrology,General Medicine
Reference58 articles.
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2. Primary hyperoxaluria type 1: Genotypic and phenotypic heterogeneity
3. Human peroxisomal l-alanine: glyoxylate aminotransferase. Evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codon
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