Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.31932/fullpdf
Reference12 articles.
1. Relevance of vitamins, homocysteine and other metabolites in neuropsychiatric disorders
2. Reversible dementia in an adolescent with cblC disease: Clinical heterogeneity within the same family
3. Adult-onset combined methylmalonic aciduria and homocystinuria (cblC)
4. Executive dysfunction in hyperhomocystinemia responds to homocysteine-lowering treatment
5. Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset.
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2. Clinical and electroencephalogram characteristics of methylmalonic acidemia with MMACHC and MUT gene mutations;BMC Pediatrics;2024-02-14
3. Late-onset methylmalonic acidemia and homocysteinemia (cblC disease): systematic review;Orphanet Journal of Rare Diseases;2024-01-20
4. Vitamin B12 Deficiency and the Nervous System: Beyond Metabolic Decompensation—Comparing Biological Models and Gaining New Insights into Molecular and Cellular Mechanisms;International Journal of Molecular Sciences;2024-01-02
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