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 |
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Zdroj: | NPJ Parkinson's Disease; 4/18/2023, Vol. 9 Issue 1, p1-14, 14p |
Databáze: | Complementary Index |
Externí odkaz: |