Functional characterization of ClC-1 mutations from patients affected by recessive myotonia congenita presenting with different clinical phenotypes - Concepedia

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Functional characterization of ClC-1 mutations from patients affected by recessive myotonia congenita presenting with different clinical phenotypes

DOI Full Paper Access

45

Citations

28

References

2013

Year

Jean‐François Desaphy, Gianluca Gramegna, Concetta Altamura, Maria Maddalena Dinardo, Paola Imbrici, Alfred L. George, Anna Modoni, Mauro LoMonaco, Diana Conte Camerino

Experimental Neurology

References

	Year	Citations

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