The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency

Lignende værker

• Isolated 3-Methylcrotonyl-CoA Carboxylase Deficiency: Evidence for an Allele-Specific Dominant Negative Effect and Responsiveness to Biotin Therapy
  af: Baumgartner, Matthias R., et al.
  Udgivet: (2004)
• Cryptic Exon Activation by Disruption of Exon Splice Enhancer: NOVEL MECHANISM CAUSING 3-METHYLCROTONYL-CoA CARBOXYLASE DEFICIENCY
  af: Stucki, Martin, et al.
  Udgivet: (2009)
• 3-methylcrotonyl-CoA carboxylase deficiency: Clinical, biochemical, enzymatic and molecular studies in 88 individuals
  af: Grünert Sarah C, et al.
  Udgivet: (2012-05-01)
• 3-methylcrotonyl-CoA carboxylase deficiency: Clinical, biochemical, enzymatic and molecular studies in 88 individuals
  af: Grünert, Sarah C, et al.
  Udgivet: (2012)
• Is l-Carnitine Supplementation Beneficial in 3-Methylcrotonyl-CoA Carboxylase Deficiency?
  af: Thomsen, Jákup Andreas, et al.
  Udgivet: (2015)