Cloning of functional alpha propionyl CoA carboxylase and correction of enzyme deficiency in pccA fibroblasts.

समान संसाधन

• Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts.
  द्वारा: Gravel, R A, और अन्य
  प्रकाशित: (1977)
• The alpha chain of human propionyl CoA carboxylase (PCCA) mapped to chromosome 13) detects an RFLP with XmnI.
  द्वारा: Bowcock, A M, और अन्य
  प्रकाशित: (1989)
• Isolation of cDNA clones coding for the alpha and beta chains of human propionyl-CoA carboxylase: chromosomal assignments and DNA polymorphisms associated with PCCA and PCCB genes.
  द्वारा: Lamhonwah, A M, और अन्य
  प्रकाशित: (1986)
• Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts.
  द्वारा: Wolf, B, और अन्य
  प्रकाशित: (1980)
• Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”
  द्वारा: Hsia, Y. Edward, और अन्य
  प्रकाशित: (1971)