Deciphering the natural history of SCA7 in children

Autor: Bruno Leheup, Anneke J.A. Kievit, Y. Capri, Cécile Cazeneuve, P. Comet‐Didierjean, Claire Ewenczyk, David Devos, Delphine Héron, Diana Rodriguez, M. Barathon, M. Carneiro, C. Barondiot, I. Strubi‐Villaume, G. Lesca, Isabelle Audo, R. van Minkelen, Agnese Suppiej, F. Dubois, A. Curie, N. Allani‐Essid, M. G. Bah, L. Ratbi, Cyril Mignot, F. Klapczynski, Joel Victor Fluss, Alexandra Durr, C. Gitiaux, Fanny Mochel, Isabelle Meunier, J. Do Cao, Perrine Charles, S. Pichard, D. Gras, Agathe Roubertie

Publikováno v: EUROPEAN JOURNAL OF NEUROLOGY
EUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 (11), pp.2267-2276. ⟨10.1111/ene.14405⟩
European Journal of Neurology, 27(11), 2267-2276. Wiley-Blackwell Publishing Ltd
European Journal of Neurology, Vol. 27, No 11 (2020) pp. 2267-2276

International audience; BACKGROUND AND PURPOSE: Childhood-onset autosomal dominant cerebellar ataxia type 7 (SCA7) is a severe disease which leads to premature loss of ambulation and death. Early diagnosis of SCA7 is of major importance for genetic c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7c82cd877098db1f920ca565b3591e3
https://hal.science/hal-03939353

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.