P. Nokelainen
AuthID: R-00G-GWQ
1
TÃTULO: Atypical phenotypes in titinopathies explained by second titin mutations and compound heterozygosity Full Text
AUTORES: Evila, A; Vihola, A; Sarparanta, J; Raheem, O; Sandell, S; Eymard, B; Illa, I; Rojas Garcia, R; Hankiewicz, K; Negrao, L; Lopponen, T; Nokelainen, P; Karppa, M; Penttila, S; Screen, M; Suominen, T; Richard, I; Hackman, P; Udd, B;
PUBLICAÇÃO: 2013, FONTE: 18th International Congress of the World-Muscle-Society (WMS) in NEUROMUSCULAR DISORDERS, VOLUME: 23, NÚMERO: 9-10
AUTORES: Evila, A; Vihola, A; Sarparanta, J; Raheem, O; Sandell, S; Eymard, B; Illa, I; Rojas Garcia, R; Hankiewicz, K; Negrao, L; Lopponen, T; Nokelainen, P; Karppa, M; Penttila, S; Screen, M; Suominen, T; Richard, I; Hackman, P; Udd, B;
PUBLICAÇÃO: 2013, FONTE: 18th International Congress of the World-Muscle-Society (WMS) in NEUROMUSCULAR DISORDERS, VOLUME: 23, NÚMERO: 9-10
INDEXADO EM: WOS CrossRef