المؤلفون: Vilarino-Guell, C, Rajput, A, Milnerwood, A J, Shah, B, Szu-Tu, C, Trinh, J, Yu, I, Encarnacion, M, Munsie, L N, Tapia, L, Gustavsson, E K, Chou, P, Tatarnikov, I, Evans, D M, Pishotta, F T, Volta, M, Beccano-Kelly, D, Thompson, C, Lin, M K, Sherman, H E, Han, H J, Guenther, B L, Wasserman, W W, Bernard, V, Ross, C J, Appel-Cresswell, S, Stoessl, A J, Robinson, C A, Dickson, D W, Ross, O A, Wszolek, Z K, Aasly, J O, Wu, R M, Hentati, F, Gibson, R A, McPherson, P S, Girard, M, Rajput, M, Rajput, A H, Farrer, M J

العلاقة: Vilarino-Guell, C, Rajput, A, Milnerwood, A J, Shah, B, Szu-Tu, C, Trinh, J, Yu, I, Encarnacion, M, Munsie, L N, Tapia, L, Gustavsson, E K, Chou, P, Tatarnikov, I, Evans, D M, Pishotta, F T, Volta, M, Beccano-Kelly, D https://orca.cardiff.ac.uk/view/cardiffauthors/A2639853M.htmlTest orcid:0000-0003-3592-8354 orcid:0000-0003-3592-8354, Thompson, C, Lin, M K, Sherman, H E, Han, H J, Guenther, B L, Wasserman, W W, Bernard, V, Ross, C J, Appel-Cresswell, S, Stoessl, A J, Robinson, C A, Dickson, D W, Ross, O A, Wszolek, Z K, Aasly, J O, Wu, R M, Hentati, F, Gibson, R A, McPherson, P S, Girard, M, Rajput, M, Rajput, A H and Farrer, M J 2014. DNAJC13 mutations in Parkinson disease. Human Molecular Genetics 23 (7) , pp. 1794-1801. 10.1093/hmg/ddt570 https://doi.org/10.1093/hmg%2Fddt570Test

الإتاحة: https://doi.org/10.1093/hmg/ddt570Test
https://orca.cardiff.ac.uk/id/eprint/150131Test/
http://europepmc.org/abstract/med/24218364Test

المؤلفون: Tzoulis C., Engelsen B. A., Telstad W., Aasly J., Zeviani M., Winterthun S., Ferrari G., Aarseth J. H., Bindoff L. A.

المساهمون: Tzoulis, C., Engelsen, B. A., Telstad, W., Aasly, J., Zeviani, M., Winterthun, S., Ferrari, G., Aarseth, J. H., Bindoff, L. A.

مصطلحات موضوعية: Alper, Ataxia, Hepatic, Mitochondrial, POLG, Adolescent, Adult, Age of Onset, Aged, Child, DNA Polymerase gamma, DNA, DNA-Directed DNA Polymerase, Developmental Disabilitie, Diffuse Cerebral Sclerosis of Schilder, Disease Progression, Epidemiologic Method, Epilepsy, Tonic-Clonic, Female, Genotype, Heredodegenerative Disorders, Nervous System, Human, Liver Failure, Magnetic Resonance Imaging, Male, Middle Aged, Mitochondrial Disease, Mutation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/16638794; info:eu-repo/semantics/altIdentifier/wos/WOS:000238761200012; volume:129; issue:7; firstpage:1685; lastpage:1692; numberofpages:8; journal:BRAIN; http://hdl.handle.net/11577/3354339Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33745685519

الإتاحة: https://doi.org/10.1093/brain/awl097Test
http://hdl.handle.net/11577/3354339Test