A NEW CASE WITH BIOTINIDASE DEFICIENCY AND ALKAPTONURIA
Mehmet Köse(Erciyes University), Mahmut Çöker(Ege University), Serkan Kurtgöz, Mehtap Kağnıcı(Antalya Eğitim ve Araştırma Hastanesi), Sema Kalkan Uçar(Ege University), Ebru Canda(Ege University), Sara Habif(Ege University), Ferda Özkınay(Ege University), Hüseyin Önay(Austen Riggs Center), Ö. Bayındır
Unknown
January 1, 2012
Cited by 0
Related Papers
A Phase 3 Trial of Sebelipase Alfa in Lysosomal Acid Lipase Deficiency
|New England Journal of Medicine|2015|244
Vitiligo pathogenesis: autoimmune disease, genetic defect, excessive reactive oxygen species, calcium imbalance, or what else?
|Experimental Dermatology|2008|210
SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice
|The American Journal of Human Genetics|2010|118
Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey
|The Journal of Clinical Endocrinology & Metabolism|2016|99