Manic-depressive Psychosis as the Initial Symptom in Adult Siblings with Late-onset Combined Methylmalonic Aciduria and Homocystinemia, Cobalamin C Type
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference6 articles.
1. Clinical, biochemical, and molecular analysis of combined methylmalonic acidemia and hyperhomocysteinemia (cblC type) in China;Wang;J Inherit Metab Dis,2010
2. Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type;Lerner-Ellis;Nat Genet,2006
3. Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria;Liu;J Hum Genet,2010
4. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy;Shinnar;N Engl J Med,1984
5. Neuropsychiatric disturbances in presumed late-onset cobalamin C disease;Roze;Arch Neurol,2003
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