14C-propionate incorporation assay by rapid filtration in multiwell plates
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference9 articles.
1. Disorders of propionate and methylmalonate metabolism;Fenton,2001
2. Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements;Dobson;Proc. Natl. Acad. Sci. U. S. A.,2002
3. Methylmalonic aciduria: an inborn error leading to metabolic acidosis, long-chain ketonuria and hyperglycinemia;Rosenberg;N. Engl. J. Med.,1968
4. Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells;Willard;Hum. Genet.,1976
5. Heterogeneous alleles and expression of methylmalonyl CoA mutase in mut methylmalonic acidemia;Ledley;Am. J. Hum. Genet.,1990
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1. Three novel and six common mutations in 11 patients with methylmalonic acidemia;Pediatrics International;2006-02
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