Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Cristina Muntean-Firanescu"'
Autor:
Humberto Skott, Cristina Muntean-Firanescu, Luca Verrecchia, Rayomand Press, Alberto J. Espay, Martin Paucar, Göran Solders, Helena Malmgren, Per Svenningsson, Kristin Samuelsson, Carmen Cananau
Publikováno v:
Cerebellum & Ataxias
Cerebellum & Ataxias, Vol 6, Iss 1, Pp 1-7 (2019)
Cerebellum & Ataxias, Vol 6, Iss 1, Pp 1-7 (2019)
Background Friedreich ataxia (FRDA) is the most common familial ataxia syndrome in Central and Southern Europe but rare in Scandinavia. Biallelic mutations in SH3 domain and tetratricopeptide repeats 2 (SH3TC2) cause Charcot-Marie-Tooth disease type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b7585b0bcc496a3994657a659099614
https://doi.org/10.1186/s40673-019-0103-8
https://doi.org/10.1186/s40673-019-0103-8
Autor:
Skott, Humberto, Muntean-Firanescu, Cristina, Samuelsson, Kristin, Verrecchia, Luca, Svenningsson, Per, Malmgren, Helena, Cananau, Carmen, Espay, Alberto J., Press, Rayomand, Solders, Göran, Paucar, Martin
Publikováno v:
Cerebellum & Ataxias; 7/15/2019, Vol. 6 Issue 1, pN.PAG-N.PAG, 1p