Загрузка...
Fabry disease: isolation of a cDNA clone encoding human alpha-galactosidase A.
Fabry disease is an X-linked inborn error of metabolism resulting from the deficient activity of the lysosomal hydrolase, alpha-galactosidase A (alpha-Gal A; alpha-D-galactoside galactohydrolase, EC 3.2.1.22). To investigate the structure, organization, and expression of alpha-Gal A, as well as the...
Сохранить в:
| Главные авторы: | , , , , , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
1985
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC391345/ https://ncbi.nlm.nih.gov/pubmed/2997789 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|