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HARVARD Citation
Hoche, F. et al. (n.d.). Novel N‐terminal truncating CLCN1 mutation in severe becker disease. Muscle & nerve. 50 (5), pp. 866-867. [Online].
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Hoche, F. et al. (n.d.). Novel N‐terminal truncating CLCN1 mutation in severe becker disease. Muscle & nerve. 50 (5), pp. 866-867. [Online].