Potential therapy for alkaptonuria – a story of cooperation among science, clinic and patients
Andrea Zaťková, Helena Glasová, Richard Imrich
Over the past 10 years, we have witnessed an increased interest in the rare disease alkaptonuria (AKU, OMIM, No. 203500), which has a primate in...
alkaptonúria, HGD gene, metabolic disorder, nitisinone, treatment of rare diseases
newsLab 2020, 1 : 41-45
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