SCIENTIFIC LITERATURE · MED

A new Turkish family with homozygous FBXO7 truncating mutation and juvenile atypical parkinsonism.

Yalcin-Cakmakli G, Olgiati S, Quadri M, Breedveld GJ, Cortelli P, Bonifati V, Elibol B.

Parkinsonism Relat Disord · 2014-07-22

Check source for accessResearch Support, Non-U.S. Gov't; Journal Article; Case ReportsOriginal source ↗

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