Zobrazeno 1 - 3
of 3
pro vyhledávání: '"M.G. Sweeny"'
Autor:
Matilde Laura, Bryan Lecky, Julia Rankin, J. Vaughan, Aisling Carr, Mary M. Reilly, A.L. Pelayo, James M. Polke, J Wilson, Tina Nanji, M.G. Sweeny
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 85:e4.80-e4
Background Mitofusion 2 (MFN2) mutations are the most common cause of axonal Charcot-Marie-Tooth disease (CMT2). The majority are inherited in an autosomal dominant manner but recessive and semidominant kindreds have been described. We previously rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19473d54f6cef064ad59a7e038802bf9
https://doi.org/10.1136/jnnp-2014-309236.170
https://doi.org/10.1136/jnnp-2014-309236.170
Autor:
Bryan Lecky, J. Vaughan, A.S. Carr, H Houlden, Julia Rankin, Matilde Laura, Mary M. Reilly, A.L. Pelayo, James M. Polke, M.G. Sweeny
Publikováno v:
Neuromuscular Disorders. 24:S21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5014e39dfd7d64a64675745d5393f227
https://doi.org/10.1016/s0960-8966(14)70068-9
https://doi.org/10.1016/s0960-8966(14)70068-9
Autor:
Cristoforo Morocutti, Nicholas W. Wood, Liana Veneziano, Marina Frontali, M.G. Sweeny, G. Sabbadini, Paola Giunti, Maria Spadaro
Publikováno v:
Journal of the Neurological Sciences. 150:S314
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c46adab71e19a5553eecb525d930e268
https://doi.org/10.1016/s0022-510x(97)86434-9
https://doi.org/10.1016/s0022-510x(97)86434-9