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Primary, secondary, and coincidental types of myoadenylate deaminase deficiency

✍ Scribed by William N. Fishbein


Book ID
101393472
Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
104 KB
Volume
45
Category
Article
ISSN
0364-5134

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Genetic characteristics of myoadenylate
✍ H. T. F. M. Verzijl; Dr. B. G. M. van Engelen; J. A. F. M. Luyten; G. C. H. Stee πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 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