Literature DB >> 7353607

Molecular basis for genetic complementation in propionyl CoA carboxylase deficiency.

B Wolf.   

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Year:  1980        PMID： 7353607     DOI： 10.1016/0014-4827(80)90147-0

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN： 0014-4827            Impact factor:   3.905


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  3 in total

Review 1.  The biotin-dependent carboxylase deficiencies.

Authors:  B Wolf; G L Feldman
Journal:  Am J Hum Genet       Date:  1982-09       Impact factor: 11.025

2.  Assignment of the alpha and beta chains of human propionyl-CoA carboxylase to genetic complementation groups.

Authors:  A M Lam Hon Wah; K F Lam; F Tsui; B Robinson; M E Saunders; R A Gravel
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

3.  Biochemical characterization of biotin-responsive multiple carboxylase deficiency: heterogeneity within the bio genetic complementation group.

Authors:  G L Feldman; Y E Hsia; B Wolf
Journal:  Am J Hum Genet       Date:  1981-09       Impact factor: 11.025
  3 in total

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