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Results 1 - 10 of 18 for mcds
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  1. 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 ...
  2. ... 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 ...
  3. ... 16(1):27-33. doi: 10.1097/01.mcd.0000228418.74413.52. Citation on PubMed Kristiansen M, ...
  4. ... Jul;24(3):89-94. doi: 10.1097/MCD.0000000000000077. Citation on PubMed or Free article on ...
  5. ... 15(3):171-174. doi: 10.1097/01.mcd.0000220603.09661.7e. Citation on PubMed Lehalle D, ...
  6. ... Jan;21(1):11-14. doi: 10.1097/MCD.0b013e32834af5a7. Citation on PubMed Asseidat I, Kaufman LM. ...
  7. ... 15(2):55-64. doi: 10.1097/01.mcd.0000198926.01706.33. Citation on PubMed van der ...
  8. ... Apr;22(2):76-80. doi: 10.1097/MCD.0b013e32835fff39. Citation on PubMed Gregersen PA, Savarirayan R. ...
  9. ... Oct;27(4):148-150. doi: 10.1097/MCD.0000000000000237. No abstract available. Citation on PubMed Miyake ...
  10. ... 15(2):75-9. doi: 10.1097/01.mcd.0000184972.76657.e1. Citation on PubMed
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