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dc.contributor.author | Claramunt, R. | es_ES |
dc.contributor.author | Pedrola, L. | es_ES |
dc.contributor.author | Sevilla, T. | es_ES |
dc.contributor.author | López de Munaín, A. | es_ES |
dc.contributor.author | Berciano, J. | es_ES |
dc.contributor.author | Cuesta, A. | es_ES |
dc.contributor.author | Sánchez-Navarro, B. | es_ES |
dc.contributor.author | Millán, J. M. | es_ES |
dc.contributor.author | Saifi, G.M. | es_ES |
dc.contributor.author | Lupski, J.R. | es_ES |
dc.contributor.author | Vilchez, J.J. | es_ES |
dc.contributor.author | Espinós-Armero, Carmen Ángeles | es_ES |
dc.contributor.author | Palau, F. | es_ES |
dc.date.accessioned | 2024-01-03T19:04:10Z | |
dc.date.available | 2024-01-03T19:04:10Z | |
dc.date.issued | 2005-04 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/201424 | |
dc.description.sponsorship | We are grateful for the kind collaboration of patients and families. We also thank Dr E Nelis and Dr V Timmerman for providing DNA samples from family PN860. This work was supported by Spanish Ministry of Science and Technology grants SAF2000-0082-C02-01 and SAF2003-00135, Fundacio¿ ``la Caixa¿¿ grant 02-004, Instituto de Salud Carlos III grant G03/56 for the Spanish Network on Cerebellar Ataxias, and the GIS-Maladies Rares Consortium on Autosomal Recessive CMT. RC is a predoctoral fellow receiving the Fundacio¿ ``la Caixa¿¿ grant and LP is a recipient of a predoctoral fellowship from the Spanish Ministry of Science and Technology. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | BMJ | es_ES |
dc.relation.ispartof | Journal of Medical Genetics | es_ES |
dc.rights | Reconocimiento - No comercial (by-nc) | es_ES |
dc.subject.classification | BIOLOGIA CELULAR | es_ES |
dc.title | Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1136/jmg.2004.022178 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/ISCIII//G03%2F56/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICYT//SAF2003-00135/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICYT//SAF2000-0082-C02-01/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural - Escola Tècnica Superior d'Enginyeria Agronòmica i del Medi Natural | es_ES |
dc.description.bibliographicCitation | Claramunt, R.; Pedrola, L.; Sevilla, T.; López De Munaín, A.; Berciano, J.; Cuesta, A.; Sánchez-Navarro, B.... (2005). Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect. Journal of Medical Genetics. 42(4):358-365. https://doi.org/10.1136/jmg.2004.022178 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1136/jmg.2004.022178 | es_ES |
dc.description.upvformatpinicio | 358 | es_ES |
dc.description.upvformatpfin | 365 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 42 | es_ES |
dc.description.issue | 4 | es_ES |
dc.identifier.eissn | 0022-2593 | es_ES |
dc.identifier.pmid | 15805163 | es_ES |
dc.identifier.pmcid | PMC1736030 | es_ES |
dc.relation.pasarela | S\505661 | es_ES |
dc.contributor.funder | Instituto de Salud Carlos III | es_ES |
dc.contributor.funder | GIS-Institut des Maladies Rares | es_ES |
dc.contributor.funder | Ministerio de Ciencia y Tecnología | es_ES |
dc.contributor.funder | Fundació Bancària Caixa d'Estalvis i Pensions de Barcelona | es_ES |