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Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvement. [electronic resource] by
- Fernández-Marmiesse, Ana
- Carrascosa-Romero, M Carmen
- Alfaro Ponce, Blanca
- Nascimento, Andres
- Ortez, Carlos
- Romero, Norma
- Palacios, Lourdes
- Jimenez-Mallebrera, Cecilia
- Jou, Cristina
- Gouveia, Sofía
- Couce, María L
Producer: 20180215
In:
Neuromuscular disorders : NMD vol. 27
Availability: No items available.
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