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Mapping the T helper cell response to acid α-glucosidase in Pompe mice
Pompe disease is a neuromuscular disease caused by an inherited deficiency of the lysosomal enzyme acid α-glucosidase (GAA). The resulting accumulation of glycogen causes muscle weakness with the severe form of the disease resulting in death by cardiorespiratory failure in the first year of life. Th...
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| Main Authors: | , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2012
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3574558/ https://ncbi.nlm.nih.gov/pubmed/22494547 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2012.03.009 |
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