Title : Modification of primers for GRHPR genotyping: avoiding allele dropout by single nucleotide polymorphisms and homology sequence.

Pub. Date : 2008 Dec

PMID : 18982322






2 Functional Relationships(s)
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1 Primary hyperoxaluria type 2 (PH2) is a rare inherited disease caused by overproduction of endogenous oxalate due to mutations in the glyoxylate/hydroxypyruvate reductase (GRHPR) gene. Oxalates glyoxylate and hydroxypyruvate reductase Homo sapiens
2 Primary hyperoxaluria type 2 (PH2) is a rare inherited disease caused by overproduction of endogenous oxalate due to mutations in the glyoxylate/hydroxypyruvate reductase (GRHPR) gene. Oxalates glyoxylate and hydroxypyruvate reductase Homo sapiens