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Tiêu đề: |
The Metabolic and Molecular Bases of Inherited Disease |
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2. Engel AG HR. Engel AG F-AC, ed. Acid maltase deficiency. McGraw- Hill; 1996 |
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Tiêu đề: |
Acid maltase deficiency |
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3. Wenger DA CS, Liu S-L. Insights into the diagnosis and treatment of lysosomal storage diseases Arch Neurol. 2003;3(60):322-328 |
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6. Sugie K YA, Murayama K et al. Clinicopathological features of genetically confirmed Danon diease. Nerology. 2002;58(12):1773-8 |
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7. Meikle PJ HJ, Clague AE et all. Prevalence of lysosomal storage disorders. Jama J Am Med Assoc. 1999;3(281):249-254 |
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Tiêu đề: |
Jama J Am Med Assoc |
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8. M B. variable clinical presentation in lysosomal storage disorders. J Inherit Metab Dis. 2001;24 Suppl(2):47-51 |
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Tiêu đề: |
J Inherit Metab Dis |
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9. Gal A SE, Rohard I. The genetic basic of Fabry disease. Fabry disease: perspectives from 5 years of FOS. Oxford PharmaGenesis; 2006 |
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Tiêu đề: |
The genetic basic of Fabry disease |
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10. Armin Mokhtariye LH-N, Abdol-Reza Varasteh et al. Diagnostic methods for Lysosomal Storage Disease. Rep Biochem Mol Biol 2019;7(2):119-128 |
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Rep Biochem Mol Biol |
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11. María Alejandra Puentes-Tellez PAL-Bea. A perspective on research, diagnosis, and management of lysosomal storage disorders in Colombia.Elsevier. Ltd; 2020. https://doi.org/10.1016/j.heliyon.2020.e03635Luận án tiến sĩ Y học |
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