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The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome
Triple A syndrome is a human autosomal recessive disorder characterized by an unusual array of tissue-specific defects. Triple A syndrome arises from mutations in a WD-repeat protein of unknown function called ALADIN (also termed Adracalin or AAAS). We showed previously that ALADIN localizes to nucl...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The National Academy of Sciences
2003
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC156285/ https://ncbi.nlm.nih.gov/pubmed/12730363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1031047100 |
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