P. Nokelainen
AuthID: R-00G-GWQ
1
TITLE: Atypical phenotypes in titinopathies explained by second titin mutations and compound heterozygosity Full Text
AUTHORS: 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;
PUBLISHED: 2013, SOURCE: 18th International Congress of the World-Muscle-Society (WMS) in NEUROMUSCULAR DISORDERS, VOLUME: 23, ISSUE: 9-10
AUTHORS: 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;
PUBLISHED: 2013, SOURCE: 18th International Congress of the World-Muscle-Society (WMS) in NEUROMUSCULAR DISORDERS, VOLUME: 23, ISSUE: 9-10
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