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| dc.contributor.author | Medico-Salsench, Eva | |
| dc.contributor.author | Maroofian, Reza | |
| dc.contributor.author | Deng, Ruizhi | |
| dc.contributor.author | Lanko, Kristina | |
| dc.contributor.author | Nikoncuk, Anita | |
| dc.contributor.author | Pérez, Belén | |
| dc.contributor.author | Sánchez-Lijarcio, Obdulia | |
| dc.contributor.author | Ibáñez-Mico, Salvador | |
| dc.contributor.author | Wojcik, Antonina | |
| dc.contributor.author | Vargas, Marcelo | |
| dc.contributor.author | Abbas-Al-Sannaa, Nouriya | |
| dc.contributor.author | Girgis, Marian-Y | |
| dc.contributor.author | Silveira, Tainá-Regina-Damaceno | |
| dc.contributor.author | Bauer, Peter | |
| dc.contributor.author | Schroeder, Audrey | |
| dc.contributor.author | Fong, Chin-To | |
| dc.contributor.author | Begtrup, Amber | |
| dc.contributor.author | Babaei, Meisam | |
| dc.contributor.author | Toosi, Mehran-Beiraghi | |
| dc.contributor.author | Ashrafzadeh, Farah | |
| dc.contributor.author | Imannezhad, Shima | |
| dc.contributor.author | Doosti, Mohammad | |
| dc.contributor.author | Ahangari, Najmeh | |
| dc.contributor.author | Najarzadeh-Torbati, Paria | |
| dc.contributor.author | Ghayoor-Karimiani, Ehsan | |
| dc.contributor.author | Murphy, David | |
| dc.contributor.author | Cali, Elisa | |
| dc.contributor.author | Kaya, Ibrahim-H | |
| dc.contributor.author | Almuhaizea, Mohammad | |
| dc.contributor.author | Colak, Dilek | |
| dc.contributor.author | Cardona-Londoño, Kelly-J | |
| dc.contributor.author | Arold, Stefan-T | |
| dc.contributor.author | Houlden, Henry | |
| dc.contributor.author | Bertoli-Avella, Aida | |
| dc.contributor.author | Kaya, Namik | |
| dc.contributor.author | Barakat, Tahsin-Stefan | |
| dc.date.accessioned | 2025-05-06T10:40:20Z | |
| dc.date.available | 2025-05-06T10:40:20Z | |
| dc.date.issued | 2021 | |
| dc.identifier.citation | Medico Salsench E, Maroofian R, Deng R, Lanko K, Nikoncuk A, Pérez B, et al. Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder. Brain. 29 de noviembre de 2021;144(10):e85. | |
| dc.identifier.issn | 1460-2156 | |
| dc.identifier.uri | https://sms.carm.es/ricsmur/handle/123456789/18811 | |
| dc.language.iso | eng | |
| dc.publisher | Oxford University Press | |
| dc.rights | Atribución-NoComercial-SinDerivadas 4.0 España | |
| dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | * |
| dc.subject.mesh | Brain Diseases | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Mutation/genetics | |
| dc.subject.mesh | Phenotype | |
| dc.title | Expanding the mutational landscape and clinical phenotype of the YIF1B related brain disorder | |
| dc.type | info:eu-repo/semantics/article | |
| dc.identifier.pmid | 34373908 | |
| dc.relation.publisherversion | https://dx.doi.org/10.1093/brain/awab297 | |
| dc.type.version | info:eu-repo/semantics/publishedVersion | |
| dc.identifier.doi | 10.1093/brain/awab297 | |
| dc.journal.title | Brain | |
| dc.identifier.essn | 0006-8950 |