Molybdenum cofactor deficiency: review of 12 cases (MoCD and review).

Bayram, Erhan; Topcu, Yasemin; Karakaya, Pakize; Yis, Uluc; Cakmakci, Handan; Ichida, Kimiyoshi; Kurul, Semra Hiz

Bayram, Erhan; Topcu, Yasemin; Karakaya, Pakize; Yis, Uluc; Cakmakci, Handan; Ichida, Kimiyoshi; Kurul, Semra Hiz.

Affiliation

Bayram E; Dokuz Eylul University Hospital, Department of Pediatrics, Division of Pediatric Neurology, 35340 Balcova, Izmir, Turkey. dr.erhanbayram@yahoo.com

Eur J Paediatr Neurol ; 17(1): 1-6, 2013 Jan.

Article in En | MEDLINE | ID: mdl-23122324

Subject(s)

Metal Metabolism, Inborn Errors/diagnosis; Carbon-Carbon Lyases; Female; Humans; Infant, Newborn; Metal Metabolism, Inborn Errors/genetics; Metal Metabolism, Inborn Errors/physiopathology; Molybdoferredoxin/genetics; Nuclear Proteins/genetics; Sulfurtransferases/genetics

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Full text: 1 Database: MEDLINE Main subject: Metal Metabolism, Inborn Errors Limits: Female / Humans / Newborn Language: En Year: 2013 Type: Article

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Full text: 1 Database: MEDLINE Main subject: Metal Metabolism, Inborn Errors Limits: Female / Humans / Newborn Language: En Year: 2013 Type: Article