作者: C R Zerez , K R Tanaka
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摘要: The delineation of specific erythrocyte glycolytic enzyme defects during the past three decades has clarified hitherto unexplained hereditary hemolytic syndromes. enzymopathies have proven to be important, not as a public health problem, but because investigation these experimental models nature provided information increase our understanding control glycolysis and interrelationships Rapoport-Luebering shunt, mechanism hemolysis, ageing, role isozymes in various organs, genetic structure/function. application ever improving techniques recombinant DNA should yield bonanza new improve comprehension pathogenesis heterogeneity disorders well provide increased knowledge regulation enzymes. It an exciting era.