Add to ORKG© 2014 Habbal et al.Alkaptonuria is often diagnosed clinically with episodes of dark urine, biochemically by the accumulation of peripheral homogentisic acid and molecularly by the presence of mutations in the homogentisate 1,2-dioxygenase gene (HGD). Alk
Alkaptonuria caused by compound heterozygote mutations: Alkaptonuria is a rare autosomal recessive d...
Alkaptonuria (AKU) is an ultra-rare metabolic disease caused by the accumulation of homogentisic aci...
Alkaptonuria (AKU) is an inborn error of metabolism caused by the deficiency of homogentisate 1,2-di...
Alkaptonuria is often diagnosed clinically with episodes of dark urine, biochemically by the accumul...
Alkaptonuria is often diagnosed clinically with episodes of dark urine, biochemically by the accumul...
SummaryAlkaptonuria (AKU), a rare hereditary disorder of phenylalanine and tyrosine catabolism, was ...
Alkaptonuria (AKU) is a rare metabolic disorder caused by a deficient enzyme in the tyrosine degrada...
Alkaptonuria (AKU) is a disorder of phenylalanine/tyrosine metabolism due to a defect in the enzyme...
Alkaptonuria is an ultra-rare autosomal recessive disease developed from the lack of homogentisate 1...
Two methods are described for homogentisic acid (HGA) determination in dried urine spots (DUS) on pa...
the mediastinal mass of a patient with alkaptonuria Alkaptonuria (AKU) is a rare autosomal recessive...
Alkaptonuria is an extremely rare condition, which is due to a defect in protein metabolism. The mos...
Abstract Alkaptonuria is a rare autosomal recessive inherited disorder of tyrosine metabolism, which...
Alkaptonuria (AKU) is a rare autosomal recessive disorder caused by mutations within a gene coding f...
Alkaptonuria is an inherited disease caused by homogentisate 1,2-dioxygenase (HGD) deficiency. Circu...
Alkaptonuria caused by compound heterozygote mutations: Alkaptonuria is a rare autosomal recessive d...
Alkaptonuria (AKU) is an ultra-rare metabolic disease caused by the accumulation of homogentisic aci...
Alkaptonuria (AKU) is an inborn error of metabolism caused by the deficiency of homogentisate 1,2-di...
Alkaptonuria is often diagnosed clinically with episodes of dark urine, biochemically by the accumul...
Alkaptonuria is often diagnosed clinically with episodes of dark urine, biochemically by the accumul...
SummaryAlkaptonuria (AKU), a rare hereditary disorder of phenylalanine and tyrosine catabolism, was ...
Alkaptonuria (AKU) is a rare metabolic disorder caused by a deficient enzyme in the tyrosine degrada...
Alkaptonuria (AKU) is a disorder of phenylalanine/tyrosine metabolism due to a defect in the enzyme...
Alkaptonuria is an ultra-rare autosomal recessive disease developed from the lack of homogentisate 1...
Two methods are described for homogentisic acid (HGA) determination in dried urine spots (DUS) on pa...
the mediastinal mass of a patient with alkaptonuria Alkaptonuria (AKU) is a rare autosomal recessive...
Alkaptonuria is an extremely rare condition, which is due to a defect in protein metabolism. The mos...
Abstract Alkaptonuria is a rare autosomal recessive inherited disorder of tyrosine metabolism, which...
Alkaptonuria (AKU) is a rare autosomal recessive disorder caused by mutations within a gene coding f...
Alkaptonuria is an inherited disease caused by homogentisate 1,2-dioxygenase (HGD) deficiency. Circu...
Alkaptonuria caused by compound heterozygote mutations: Alkaptonuria is a rare autosomal recessive d...
Alkaptonuria (AKU) is an ultra-rare metabolic disease caused by the accumulation of homogentisic aci...
Alkaptonuria (AKU) is an inborn error of metabolism caused by the deficiency of homogentisate 1,2-di...