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pro vyhledávání: '"Loiuse A. Dionne"'
Autor:
Kathryn H. Morelli, Kevin L. Seburn, David G. Schroeder, Emily L. Spaulding, Loiuse A. Dionne, Gregory A. Cox, Robert W. Burgess
Publikováno v:
Cell Reports, Vol 18, Iss 13, Pp 3178-3191 (2017)
Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous group of inherited polyneuropathies. Mutations in 80 genetic loci can cause forms of CMT, resulting in demyelination and axonal dysfunction. The clinical presentation, in
Externí odkaz:
https://doaj.org/article/75c1f25d43654c798eae312e468f7433
Autor:
Loiuse A. Dionne, Robert W. Burgess, Kathryn H. Morelli, David G. Schroeder, Emily Spaulding, Gregory A. Cox, Kevin L. Seburn
Publikováno v:
Cell Reports, Vol 18, Iss 13, Pp 3178-3191 (2017)
Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous group of inherited polyneuropathies. Mutations in 80 genetic loci can cause forms of CMT, resulting in demyelination and axonal dysfunction. The clinical presentation, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::269abc8c0f390bc6a0e50f7ace6374b8
https://doi.org/10.1016/j.celrep.2017.03.009
https://doi.org/10.1016/j.celrep.2017.03.009