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- Holocarboxylase synthetase deficiency is an inherited disorder in which the body is unable to use the vitamin biotin effectively. This disorder is classified as a multiple ...
- ... decarboxylase Malonic aciduria Malonyl-coenzyme A decarboxylase deficiency MCD deficiency Genetic Testing Registry: Deficiency of malonyl-CoA ... Morrell JC, Wanders RJ, Matalon R, Gould SJ. MCD encodes peroxisomal and cytoplasmic forms of malonyl-CoA ...
- ... 16(1):27-33. doi: 10.1097/01.mcd.0000228418.74413.52. Citation on PubMed Kristiansen M, ...
- ... Jul;24(3):89-94. doi: 10.1097/MCD.0000000000000077. Citation on PubMed or Free article on ...
- ... 15(3):171-174. doi: 10.1097/01.mcd.0000220603.09661.7e. Citation on PubMed Lehalle D, ...
- ... Jan;21(1):11-14. doi: 10.1097/MCD.0b013e32834af5a7. Citation on PubMed Asseidat I, Kaufman LM. ...
- ... 15(2):55-64. doi: 10.1097/01.mcd.0000198926.01706.33. Citation on PubMed van der ...
- ... Apr;22(2):76-80. doi: 10.1097/MCD.0b013e32835fff39. Citation on PubMed Gregersen PA, Savarirayan R. ...
- ... Oct;27(4):148-150. doi: 10.1097/MCD.0000000000000237. No abstract available. Citation on PubMed Miyake ...
- ... 15(2):75-9. doi: 10.1097/01.mcd.0000184972.76657.e1. Citation on PubMed