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dc.contributor | Universitat de Barcelona |
---|---|
dc.contributor.author | Brito, Sara |
dc.contributor.author | Thompson, Kyle |
dc.contributor.author | Campistol Plana, Jaume |
dc.contributor.author | Colomer, Jaume |
dc.contributor.author | Hardy, Steven A. |
dc.contributor.author | Langping, He |
dc.contributor.author | Fernández Marmiesse, Ana |
dc.contributor.author | Palacios, Lourdes |
dc.contributor.author | Jou, Cristina |
dc.contributor.author | Jiménez-Mallebrera, Cecilia |
dc.contributor.author | Armstrong i Morón, Judith |
dc.contributor.author | Montero, Raquel |
dc.contributor.author | Artuch Iriberri, Rafael |
dc.contributor.author | Tischner, Christin |
dc.contributor.author | Wenz, Tina |
dc.contributor.author | McFarland, Robert |
dc.contributor.author | Taylor, Robert W. |
dc.date | 2017-01-20T17:55:17Z |
dc.date | 2017-01-20T17:55:17Z |
dc.date | 2015-03-23 |
dc.date | 2017-01-20T17:55:17Z |
dc.identifier.citation | 1664-8021 |
dc.identifier.citation | 658069 |
dc.identifier.uri | http://hdl.handle.net/2445/105930 |
dc.format | 9 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | Frontiers Media |
dc.relation | Reproducció del document publicat a: https://doi.org/10.3389/fgene.2015.00102 |
dc.relation | Frontiers in Genetics, 2015, vol. 6, num. 102, p. 102 |
dc.relation | https://doi.org/10.3389/fgene.2015.00102 |
dc.rights | cc-by (c) Brito, Sara et al., 2015 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.rights | http://creativecommons.org/licenses/by/3.0/es |
dc.subject | Infants |
dc.subject | Malalties cerebrals |
dc.subject | Mitocondris |
dc.subject | Genètica mèdica |
dc.subject | Children |
dc.subject | Brain diseases |
dc.subject | Mitochondria |
dc.subject | Medical genetics |
dc.title | Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |