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46. Myotonia levior is a chloride channel disorder. Lehmann-Horn F; Mailänder V; Heine R; George AL Hum Mol Genet; 1995 Aug; 4(8):1397-402. PubMed ID: 7581380 [TBL] [Abstract][Full Text] [Related]
47. New mutation of the Na channel in the severe form of potassium-aggravated myotonia. Kubota T; Kinoshita M; Sasaki R; Aoike F; Takahashi MP; Sakoda S; Hirose K Muscle Nerve; 2009 May; 39(5):666-73. PubMed ID: 19347921 [TBL] [Abstract][Full Text] [Related]
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52. New classification and treatment for myotonic disorders. Kurihara T Intern Med; 2005 Oct; 44(10):1027-32. PubMed ID: 16293911 [TBL] [Abstract][Full Text] [Related]
53. Potassium uptake in muscle during paramyotonic weakness. Moxley RT; Ricker K; Kingston WJ; Böhlen R Neurology; 1989 Jul; 39(7):952-5. PubMed ID: 2500620 [TBL] [Abstract][Full Text] [Related]
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56. Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel. Mitrović N; George AL; Lerche H; Wagner S; Fahlke C; Lehmann-Horn F J Physiol; 1995 Aug; 487(1):107-14. PubMed ID: 7473241 [TBL] [Abstract][Full Text] [Related]
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59. Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita. Ptácek LJ; George AL; Barchi RL; Griggs RC; Riggs JE; Robertson M; Leppert MF Neuron; 1992 May; 8(5):891-7. PubMed ID: 1316765 [TBL] [Abstract][Full Text] [Related]
60. New phenotype and neonatal onset of sodium channel myotonia in a child with a novel mutation of SCN4A gene. Fusco C; Frattini D; Salerno GG; Canali E; Bernasconi P; Maggi L Brain Dev; 2015 Oct; 37(9):891-3. PubMed ID: 25735906 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]