A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification
2006 ◽
Vol 16
(5)
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pp. 321-324
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2009 ◽
Vol 31
(10)
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pp. 758-762
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1996 ◽
Vol 97
(7)
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pp. 1780-1784
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2016 ◽
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2018 ◽
Vol 12
(1)
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pp. e0006192
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