Author:
Vatanavicharn Nithiwat,Champattanachai Voraratt,Liammongkolkul Somporn,Sawangareetrakul Phannee,Keeratichamroen Siriporn,Ketudat Cairns James R.,Srisomsap Chantragan,Sathienkijkanchai Achara,Shotelersuk Vorasuk,Kamolsilp Mahattana,Wattanasirichaigoon Duangrurdee,Svasti Jisnuson,Wasant Pornswan
Funder
Chulabhorn Research Institute
Thailand Research Fund
Siriraj Chalermprakiat Fund
Mahidol University
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference33 articles.
1. Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression;Willard;J. Clin. Invest.,1980
2. Disorders of propionate and methylmalonate metabolism;Fenton,2001
3. Long-term follow-up of 77 patients with isolated methylmalonic aciduria;Baumgartner;J. Inherit. Metab. Dis.,1995
4. The neurological outcome of methylmalonic acidaemia;Nicolaides;Arch. Dis. Child.,1998
5. Long-term outcome in methylmalonic acidurias is influenced by the underlying defect (mut0, mut-, cblA, cblB);Hörster;Pediatr. Res.,2007
Cited by
29 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