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dc.contributor | Universitat de Barcelona |
---|---|
dc.contributor.author | Barrientos Rubio, Antoni |
dc.contributor.author | Volpini Bertrán, Víctor |
dc.contributor.author | Casademont i Pou, Jordi |
dc.contributor.author | Genís, David |
dc.contributor.author | Manzanares, Josep-Maria |
dc.contributor.author | Ferrer, Isidro (Ferrer Abizanda) |
dc.contributor.author | Corral, Jordi |
dc.contributor.author | Cardellach, Francesc |
dc.contributor.author | Urbano Márquez, A. (Álvaro) |
dc.contributor.author | Estivill, Xavier, 1955- |
dc.contributor.author | Nunes Martínez, Virginia |
dc.date | 2009-05-15T08:20:19Z |
dc.date | 2009-05-15T08:20:19Z |
dc.date | 1996 |
dc.identifier.citation | 0021-9738 |
dc.identifier.citation | 114902 |
dc.identifier.uri | http://hdl.handle.net/2445/8304 |
dc.format | 7 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | American Society for Clinical Investigation |
dc.relation | Reproducció del document publicat a http://dx.doi.org/10.1172/JCI118581 |
dc.relation | Journal of Clinical Investigation, 1996, vol. 97, núm. 7, p. 1570¿1576. |
dc.relation | http://dx.doi.org/10.1172/JCI118581 |
dc.rights | (c) The American Society for Clinical Investigation, 1996 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.subject | Mitocondris |
dc.subject | Degeneració del sistema nerviòs |
dc.subject | Genètica humana |
dc.subject | Neurodegenerative diseases |
dc.subject | OXPHOS |
dc.subject | Autosomal recessive inheritance |
dc.subject | Linkage |
dc.subject | DIDMOAD |
dc.title | A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |