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P.3.11 Atypical phenotypes in titinopathies explained by second titin mutations and compound heterozygosity
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.,Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.436
Date:
October, 2013
File:
PDF, 58 KB
english, 2013