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Gene therapy for haemophilia

The ultimate goal of gene therapy is the replacement of a defective gene sequence with a corrected version to eliminate disease for the lifetime of the patient. This challenging task is not yet accomplished, however significant progress is evident. An initial spate of clinical trials attempting the...

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Detalles Bibliográficos
Autores principales: Murphy, Samuel L, High, Katherine A
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408641/
https://www.ncbi.nlm.nih.gov/pubmed/18275425
http://dx.doi.org/10.1111/j.1365-2141.2007.06942.x