Molecular phenotypes of mitochondrial dysfunction in clinically non-manifesting heterozygous PRKN variant carriers.

Autor: Castelo Rueda, Maria Paulina, Zanon, Alessandra, Gilmozzi, Valentina, Lavdas, Alexandros A., Raftopoulou, Athina, Delcambre, Sylvie, Del Greco M, Fabiola, Klein, Christine, Grünewald, Anne, Pramstaller, Peter P., Hicks, Andrew A., Pichler, Irene
Zdroj: NPJ Parkinson's Disease; 4/18/2023, Vol. 9 Issue 1, p1-14, 14p
Databáze: Complementary Index
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