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Autor:
Trinh, Joanne, Hicks, Andrew A., Koenig, Inke R., Delcambre, Sylvie, Lueth, Theresa, Schaake, Susen, Wasner, Kobi, Ghelfi, Jenny, Borsche, Max, Vilarino-Guell, Carles, Hentati, Faycel, Germer, Elisabeth L., Bauer, Peter, Takanashi, Masashi, Kostic, Vladimir, Lang, Anthony E., Brueggeman, Norbert, Pramstaller, Peter P., Pichler, Irene, Rajput, Alex, Hattori, Nobutaka, Farrer, Matthew J., Lohmann, Katja, May, Patrick, Weissensteiner, Hansi, Klein, Christine, Grünewald, Anne
Biallelic mutations in PINK1 and PRKN cause recessively inherited Parkinson's disease (PD). Though some studies suggest that PINK1/PRKN monoallelic mutations may not contribute to risk, deep phenotyping assessment showed that PINK1 or PRKN monoalleli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2658::121dd3968ca37ab17c95da10f55e1c37
http://orbilu.uni.lu/handle/10993/51280
http://orbilu.uni.lu/handle/10993/51280