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Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.

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Description scientific article published on 22 December 2015
Author/s

author: Christian Krarup  Luigi D'Argenzio  Roope Mannikko  Hilary Vallance  Nigel G Laing  Clara van Karnebeek  Michael T Gabbett  Karen Joan Suetterlin  Xin Cynthia Ye  Michael Hanna  John Vissing  Francesco Muntoni  Erik-Jan Kamsteeg  Nanna Witting  Michael G Thor 

Publication date December 22, 2015
Language English
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