Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis type II - Hunter syndrome.

Autor: Chiong MA; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, 625 Pedro Gil St., Ermita, Manila, 1000, Philippines. mdchiong1@up.edu.ph.; Department of Pediatrics, University of the Philippines-Philippine General Hospital, Manila, Philippines. mdchiong1@up.edu.ph.; Department of Pediatrics, College of Medicine, University of Santo Tomas, Manila, Philippines. mdchiong1@up.edu.ph., Canson DM; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, 625 Pedro Gil St., Ermita, Manila, 1000, Philippines., Abacan MA; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, 625 Pedro Gil St., Ermita, Manila, 1000, Philippines.; Department of Pediatrics, University of the Philippines-Philippine General Hospital, Manila, Philippines., Baluyot MM; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, 625 Pedro Gil St., Ermita, Manila, 1000, Philippines.; Department of Pediatrics, University of the Philippines-Philippine General Hospital, Manila, Philippines., Cordero CP; Department of Clinical Epidemiology, College of Medicine, University of the Philippines, Manila, Philippines., Silao CL; Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, 625 Pedro Gil St., Ermita, Manila, 1000, Philippines.; Department of Pediatrics, University of the Philippines-Philippine General Hospital, Manila, Philippines.

Publikováno v: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2017 Jan 11; Vol. 12 (1), pp. 7. Date of Electronic Publication: 2017 Jan 11.