Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation
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| Description | scientific article published on 26 November 2019 |
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author: Marisol Sampedro-Castañeda Roope Mannikko Michael Hanna |
| Publication date | November 26, 2019 |
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