Biochemical characterization and intracellular localization of the Menkes disease protein
Menkes disease is a fatal neurodegenerative disorder of childhood due to the absence or dysfunction of a putative copper-transporting P-type ATPase encoded on the X chromosome. To elucidate the biosynthesis and subcellular localization of this protein, polyclonal antisera were generated against a ba...
Gardado en:
| Publicado en: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
National Academy of Sciences
1996
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC19489/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8943055/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.93.24.14030 |
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