טוען...
Role of βArg(211) in the Active Site of Human β-Hexosaminidase B
Tay–Sachs or Sandhoff disease results from a deficiency of either the α- or the β-subunits of β-hexosaminidase A, respectively. These evolutionarily related subunits have been grouped with the “Family 20” glycosidases. Molecular modeling of human hexosaminidase has been carried out on the basis of t...
שמור ב:
| Main Authors: | , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2000
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2910084/ https://ncbi.nlm.nih.gov/pubmed/10821697 |
| תגים: |
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