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HARVARD Citation
Jonson, P. et al. (2018). Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families. European journal of neurology. pp. 790-794. [Online].
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Jonson, P. et al. (2018). Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families. European journal of neurology. pp. 790-794. [Online].