Late-onset Pompe disease: preliminary results of enzyme replacement therapy
Pompe disease is an orphan hereditary accumulation disease associated with a deficiency of the lysosomal enzyme alglucosidase alpha. Manifestations of the disease are associated with pathological deposition of glycogen in body tissues as a result of GAA gene mutation and subsequent reduction in the...
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Main Authors: | L. P. Smertina, F. I. Ausheva, A. V. Gryaznov, D. A. Svetlakov, L. N. Kolbasin |
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Format: | Article |
Language: | Russian |
Published: |
ABV-press
2019-07-01
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Series: | Нервно-мышечные болезни |
Subjects: | |
Online Access: | https://nmb.abvpress.ru/jour/article/view/326 |
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