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pro vyhledávání: '"Madurai P. Saravanan"'
Autor:
Andrea Zatkova, Srinivasan Sakthivel, Ludevit Kadasi, Milan Surovy, Martina Nemethova, Madurai P. Saravanan
Publikováno v:
Annals of Human Genetics. 78:155-164
Alkaptonuria (AKU) is an autosomal recessive disorder; caused by the mutations in the homogentisate 1, 2-dioxygenase (HGD) gene located on Chromosome 3q13.33. AKU is a rare disorder with an incidence of 1: 250,000 to 1: 1,000,000, but Slovakia and th
Autor:
Srinivasan, Sakthivel, Andrea, Zatkova, Martina, Nemethova, Milan, Surovy, Ludevit, Kadasi, Madurai P, Saravanan
Publikováno v:
Annals of human genetics. 78(3)
Alkaptonuria (AKU) is an autosomal recessive disorder; caused by the mutations in the homogentisate 1, 2-dioxygenase (HGD) gene located on Chromosome 3q13.33. AKU is a rare disorder with an incidence of 1: 250,000 to 1: 1,000,000, but Slovakia and th