Your browser doesn't support javascript.
loading
Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiency.
Yazici, Havva; Canda, Ebru; Onay, Hüseyin; Uçar, Sema Kalkan; Habif, Sara; Çoker, Mahmut.
Affiliation
  • Yazici H; Departments of Pediatric Metabolism and Nutrition, Ege University Faculty of Medicine, Izmir, Türkiye.
  • Canda E; Departments of Pediatric Metabolism and Nutrition, Ege University Faculty of Medicine, Izmir, Türkiye.
  • Onay H; Departments of Genetic, Ege University Faculty of Medicine, Izmir, Türkiye.
  • Uçar SK; Departments of Pediatric Metabolism and Nutrition, Ege University Faculty of Medicine, Izmir, Türkiye.
  • Habif S; Departments of Biochemistry, Ege University Faculty of Medicine, Izmir, Türkiye.
  • Çoker M; Departments of Pediatric Metabolism and Nutrition, Ege University Faculty of Medicine, Izmir, Türkiye.
Turk J Pediatr ; 64(5): 946-950, 2022.
Article in En | MEDLINE | ID: mdl-36305448
Subject(s)
Key words
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amino Acid Metabolism, Inborn Errors Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Turk J Pediatr Year: 2022 Type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amino Acid Metabolism, Inborn Errors Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Turk J Pediatr Year: 2022 Type: Article