Alpers Huttenlocher syndrome a case with cerebral folate deficiency and a novel POLG1 mutation

HİŞMİ B., ÜNAL Ö., GENÇ SEL Ç., DURSUN A., SİVRİ H. S., COŞKUN T., ...More

12th International Congress of Inborn Errors of Metabolism, 3 - 06 September 2013

• Publication Type: Conference Paper
• Kocaeli University Affiliated: Yes