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Muscle & Nerve, ISSN 0148-639X, 10/2012, Volume 46, Issue 4, pp. 482 - 489
Journal Article
Experimental Neurology, ISSN 0014-4886, 03/2014, Volume 253, pp. 28 - 30
Non-dystrophic myotonias are rare diseases caused by mutations in skeletal muscle chloride and sodium ion channels with considerable phenotypic overlap between... 
Paramyotonia | SCN4A | Non-dystrophic myotonia | Myotonia | CLCN1 | PERIODIC PARALYSIS | RECESSIVE MYOTONIA | CLINICAL PHENOTYPES | DOMINANT | CONGENITA | MUSCLE CHLORIDE CHANNEL | NEUROSCIENCES | SKELETAL-MUSCLE | DISEASE | QUALITY-OF-LIFE | MUTATIONS | Phenotype | Chloride Channels - genetics | Mutation | Myotonia Congenita - genetics | Humans | non-dystrophic myotonia | myotonia | paramyotonia
Journal Article
Brain, ISSN 0006-8950, 2013, Volume 136, Issue 7, pp. 2189 - 2200
Journal Article
Journal Article
BMC NEUROLOGY, ISSN 1471-2377, 06/2019, Volume 19, Issue 1, pp. 125 - 6
Journal Article
by Lau, WL and Ko, CH and Lee, HHC and Mak, CM
HONG KONG JOURNAL OF PAEDIATRICS, ISSN 1013-9923, 04/2019, Volume 24, Issue 2, pp. 93 - 96
Non-dystrophic myotonia (NDMs) is a group of heterogenous skeletal muscle channelopathies. This entity is rare but potentially treatable. We reported two... 
Non-dystrophic myotonia | Myotonia | Paramyotonia | PEDIATRICS | Mexiletine | Myotonia congenita
Journal Article
Neurological Research, ISSN 0161-6412, 01/2016, Volume 38, Issue 1, pp. 40 - 44
Journal Article
Journal Article
Restorative neurology and neuroscience, ISSN 0922-6028, 2018, Volume 36, Issue 4, pp. 459 - 467
Journal Article