P.3.11 Atypical phenotypes in titinopathies explained by...

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.,
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Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.436
Date:
October, 2013
File:
PDF, 58 KB
english, 2013
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