Voprosy meditsinskoi khimii (ISSN 0042-8809)

Genetic complementation in the study of mechanisms of inborn errors of metabolism in man (review of the literature)

   
Baskaeva E.M.
PubMed Id: 2188424
Year: 1990 vol: 36  issue:1  pages: 13-18
Abstract: Application of genetic complementation procedure for evaluation of heterogeneity and development of a number of human inherited impairments, particularly, lysosomal storage diseases, are reviewed. The genetic complementation procedure is involved in cytobiochemical diagnosis of a number of enzymopathies as well as in studies of subunit containing enzymes reconstruction and their function.
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Reference: Baskaeva E.M., Genetic complementation in the study of mechanisms of inborn errors of metabolism in man (review of the literature), Voprosy meditsinskoi khimii, 1990, vol: 36(1), 13-18.
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