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Molecular analysis of 11 galactosemia patients.
Galactosemia is a human inborn error of galactose metabolism due to deficiency of galactose-1-phosphate uridyl transferase. In this paper, I describe the molecular analysis of genomic DNA, mRNA and protein from 11 different galactosemic patients by Southern, Northern and Western blotting. The result...
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| Autor principal: | |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
1991
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC332510/ https://ncbi.nlm.nih.gov/pubmed/1766867 |
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