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dc.contributor | Universitat de Barcelona |
---|---|
dc.contributor.author | Belmonte, Irene |
dc.contributor.author | Barrecheguren, Miriam |
dc.contributor.author | Esquinas López, Cristina |
dc.contributor.author | Rodríguez, Esther |
dc.contributor.author | Miravitlles Fernández, Marc |
dc.contributor.author | Rodriguez-Frias, Francisco |
dc.date | 2018-03-22T12:14:43Z |
dc.date | 2018-03-22T12:14:43Z |
dc.date | 2017-09 |
dc.date | 2018-03-22T12:14:43Z |
dc.identifier.citation | 1434-6621 |
dc.identifier.citation | 678835 |
dc.identifier.uri | http://hdl.handle.net/2445/121004 |
dc.format | 8 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | Walter de Gruyter GmbH & Co. KG. |
dc.relation | Reproducció del document publicat a: https://doi.org/10.1515/cclm-2016-0842 |
dc.relation | Clinical Chemistry and Laboratory Medicine, 2017, vol. 55, num. 9, p. 1276-1283 |
dc.relation | https://doi.org/10.1515/cclm-2016-0842 |
dc.rights | (c) Walter de Gruyter GmbH & Co. KG., 2017 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.subject | Cribratge genètic |
dc.subject | Errors congènits del metabolisme |
dc.subject | Malalties hereditàries |
dc.subject | ADN |
dc.subject | Sèrum |
dc.subject | Secrecions |
dc.subject | Diagnòstic |
dc.subject | Genetic screening |
dc.subject | Inborn errors of metabolism |
dc.subject | Genetic diseases |
dc.subject | DNA |
dc.subject | Serum |
dc.subject | Secretions |
dc.subject | Diagnosis |
dc.title | Genetic diagnosis of α1-antitrypsin deficiency using DNA from buccal swab and serum samples |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |