Cite
HARVARD Citation
Kostera‐Pruszczyk, A. et al. (2014). Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot–Marie–Tooth disease. Journal of the peripheral nervous system. 19 (3), pp. 242-245. [Online].
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Kostera‐Pruszczyk, A. et al. (2014). Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot–Marie–Tooth disease. Journal of the peripheral nervous system. 19 (3), pp. 242-245. [Online].