Genetic characteristics of myoadenylate
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H. T. F. M. Verzijl; Dr. B. G. M. van Engelen; J. A. F. M. Luyten; G. C. H. Stee
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Article
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1998
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John Wiley and Sons
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English
β 663 KB
Two types of myoadenylate deaminase (MAD) deficiency have been described, primary or inherited, and secondary or acquired MAD deficiency. In this study, we investigated whether secondary MAD deficiency is indeed acquired or merely coincidental. We demonstrated the same underlying molecular defect, a