Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region.
Human alpha-galactosidase A (alpha-D-galactoside galactohydrolase; EC 3.2.1.22) is a lysosomal hydrolase encoded by a gene localized to the chromosomal region Xq22. The deficient activity of this enzyme results in Fabry disease, an X chromosome-linked recessive disorder that leads to premature death...
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| Pubblicato in: | Proc Natl Acad Sci U S A |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
National Academy of Sciences
1988
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC280328/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2836863/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.85.11.3903 |
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