المؤلفون: Pons, N., Fernández-Eulate, G., Pegat, A., Théaudin, M., Guieu, R., Ripellino, P., Devedjian, M., Mace, P., Masingue, M., Léonard-Louis, S., Petiot, P., Roche, P., Bernard, E., Bouhour, F., Good, J.M., Verschueren, A., Grapperon, A.M., Salort, E., Grosset, A., Chanson, J.B., Nadaj-Pakleza, A., Bédat-Millet, A.L., Choumert, A., Barnier, A., Hamdi, G., Lesca, G., Prieur, F., Bruneel, A., Latour, P., Stojkovic, T., Attarian, S., Bonello-Palot, N.

المصدر: European journal of neurology, vol. 30, no. 7, pp. 2001-2011

مصطلحات موضوعية: Humans, Switzerland, Mutation, Charcot-Marie-Tooth Disease/genetics, Genotype, Muscular Atrophy, SORD, Charcot-Marie-Tooth, neuropathy, peripheral neuropathy

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/36943151; info:eu-repo/semantics/altIdentifier/eissn/1468-1331; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_EBAC3490A2103; https://serval.unil.ch/notice/serval:BIB_EBAC3490A210; https://serval.unil.ch/resource/serval:BIB_EBAC3490A210.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_EBAC3490A210
https://doi.org/10.1111/ene.15793
https://serval.unil.ch/resource/serval:BIB_EBAC3490A210.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_EBAC3490A2103