SCIENTIFIC LITERATURE · MED

PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family.

Olgiati S, De Rosa A, Quadri M, Criscuolo C, Breedveld GJ, Picillo M, Pappatà S, Quarantelli M, Barone P, De Michele G, Bonifati V.

Neurogenetics · 2014-05-10

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

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