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Urology, ISSN 0090-4295, 2016, Volume 100, pp. e3 - e4
Abstract Alkaptonuria is a rare autosomal recessive disorder of tyrosine metabolism. Deficiency of homogentisate 1,2 dioxygenase results in accumulation of... 
Urology | UROLOGY & NEPHROLOGY | Ochronosis - diagnosis | Ochronosis - complications | Humans | Middle Aged | Male | Alkaptonuria - complications | Alkaptonuria - diagnosis | Tyrosine
Journal Article
American Journal of Physical Medicine & Rehabilitation, ISSN 0894-9115, 02/2017, Volume 96, Issue 11, pp. e206 - e209
Journal Article
Journal of Forensic Sciences, ISSN 0022-1198, 05/2019, Volume 64, Issue 3, pp. 913 - 916
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 11/2012, Volume 1822, Issue 11, pp. 1682 - 1691
Journal Article
Journal Article
Saudi Medical Journal, ISSN 0379-5284, 12/2015, Volume 36, Issue 12, pp. 1486 - 1489
Alkaptonuria (AKU) is a rare inborn metabolic disease characterized by accumulation of homogentisic acid (HGA). Excretion of HGA in urine causes darkening of... 
MEDICINE, GENERAL & INTERNAL | Rupture, Spontaneous - surgery | Humans | Rupture, Spontaneous - complications | Adult | Male | Treatment Outcome | Alkaptonuria - complications | Achilles Tendon - injuries | Case Report
Journal Article
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