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23. Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita. Fialho D; Kullmann DM; Hanna MG; Schorge S Neuromuscul Disord; 2008 Nov; 18(11):869-72. PubMed ID: 18815035 [TBL] [Abstract][Full Text] [Related]
24. Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletion. Heine R; George AL; Pika U; Deymeer F; Rüdel R; Lehmann-Horn F Hum Mol Genet; 1994 Jul; 3(7):1123-8. PubMed ID: 7981681 [TBL] [Abstract][Full Text] [Related]
25. The skeletal muscle sodium and chloride channel diseases. Hudson AJ; Ebers GC; Bulman DE Brain; 1995 Apr; 118 ( Pt 2)():547-63. PubMed ID: 7735894 [TBL] [Abstract][Full Text] [Related]
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30. K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation. Mitrović N; George AL; Heine R; Wagner S; Pika U; Hartlaub U; Zhou M; Lerche H; Fahlke C; Lehmann-Horn F J Physiol; 1994 Aug; 478 Pt 3(Pt 3):395-402. PubMed ID: 7965854 [TBL] [Abstract][Full Text] [Related]
31. Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype. Gurgel-Giannetti J; Senkevics AS; Zilbersztajn-Gotlieb D; Yamamoto LU; Muniz VP; Pavanello RC; Oliveira AB; Zatz M; Vainzof M Muscle Nerve; 2012 Feb; 45(2):279-83. PubMed ID: 22246887 [TBL] [Abstract][Full Text] [Related]
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