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HARVARD Citation
Bryen, S. et al. (2020). Recurrent TTN metatranscript‐only c.39974–11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy. Human mutation. 41 (2), pp. 403-411. [Online].
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Bryen, S. et al. (2020). Recurrent TTN metatranscript‐only c.39974–11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy. Human mutation. 41 (2), pp. 403-411. [Online].