Author:
Aljassim Nada,Alfadhel Majid,Nashabat Marwan,Eyaid Wafa
Subject
Endocrinology,Genetics,Molecular Biology
Reference12 articles.
1. David S. Rosenblatt, David Watkins. Inherited Disorders of Folate and Cobalamin Transport and Metabolism. The Online Metabolic and Molecular Bases of Inherited Diseases. S.L. : Mc Grow Hill.
2. Baethmann M, Wendel U, Hoffmann GF, Göhlich-Ratmann G, Kleinlein B, Seiffert P, Blom H, Voit T (2000) Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiency. Germany : Neuropediatrics, Vols. 31(6):314–7.
3. Martina Huemer, Regina Mulder-Bleile,Patricie Burda,et al. clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency. J. Inherit. Metab. Dis. 2016 Jan 1; 39(1): 115–124.
4. Inborn errors of folate metabolism;Wiley,1986
5. Morphologic studies in a patient with homocystinuria due to 5,10- methylenetetrahydrofolate reductase deficiency;Kanwar;Pediatr. Res.,1976
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献