| cob(I)alamin adenosyltransferase |
[EC 2.5.1.17] a mitochondrial enzyme of the transferase class that catalyzes the transfer of an adenosyl group to cobalamin from ATP, forming the coenzyme adenosylcobalamin. Deficiency of the enzyme, an autosomal recessive trait (CblB), leads to deficiency of methylmalonyl-CoA mutase activity and results in methylmalonicacidemia.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
|---|---|
| cobalamin reductase |
either of two mitochondrial reductases that catalyze steps in the synthesis of adenosylcobalamin from hydroxocobalamin; deficiency of one or both is believed to be a cause of methylmalonicacidemia (q.v.).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| cobalophilin |
R protein.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| cobalt l. |
hard metal disease.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| cobalt p. |
poisoning from long-term excessive exposure to cobalt, seen in those who work with cobalt and formerly in beer drinkers because for years cobalt was added to beer as a foam stabilizer. Symptoms include nausea, vomiting, tinnitus, nerve deafness, and cardiomyopathy (beer-drinkers' cardiomyopathy).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|