Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A. (Q43608348)

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Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
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    Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A. (English)
    Sternberg D
    Maisonobe T
    Jurkat-Rott K
    Nicole S
    Launay E
    Chauveau D
    Lehmann-Horn F
    Hainque B
    Fontaine B
    1 June 2001
    1091-1099
    Pt 6

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