Publication | Closed Access
In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia
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Citations
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References
2008
Year
Tandem AnalysisMendelian DisorderGenetic DisorderNon-dystrophic MyotoniaGeneticsMutation DetectionMedicineMolecular BiologyMolecular GeneticsMutagenesisDisease Gene IdentificationMolecular DiagnosticsGenetic MedicineClinical Genetics
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