Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia

Detalles Bibliográficos
Autores principales: Rohrer, Jonathan D, Beck, Jonathan, Plagnol, Vincent, Gordon, Elizabeth, Lashley, Tammaryn, Revesz, Tamas, Janssen, John C, Fox, Nick C, Warren, Jason D, Rossor, Martin N, Mead, Simon, Schott, Jonathan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
PostScript
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905627/
https://www.ncbi.nlm.nih.gov/pubmed/23904625
http://dx.doi.org/10.1136/jnnp-2013-306116

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3905627/
https://www.ncbi.nlm.nih.gov/pubmed/23904625
http://dx.doi.org/10.1136/jnnp-2013-306116

Ejemplares similares