Genetics of type II glycogenosis: Assignment of the human gene for acid α-glucosidase to chromosome 17
We have studied somatic cell hybrids between thymidine kinase (EC 2.7.1.75) deficient mouse cells and human diploid fibroblasts for the expression of human acid α-glucosidase (EC 3.2.1.20). A deficiency in this enzyme is associated with the type II glycogenosis or Pompe disease. All 30 somatic cell...
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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1979
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC411610/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/388444/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.76.9.4526 |
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