A carregar...
Clinical Outcomes in Menkes Disease Patients with a Copper-Responsive ATP7A Mutation, G727R
Menkes disease is a fatal neurodegenerative disorder of infancy caused by defects in an X-linked copper transport gene, ATP7A. Evidence from a recent clinical trial indicates that favorable response to early treatment of this disorder with copper injections involves mutations that retain some copper...
Na minha lista:
| Main Authors: | , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2654537/ https://ncbi.nlm.nih.gov/pubmed/18752978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2008.06.015 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|