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pro vyhledávání: '"Lynn Langlott"'
Autor:
Martin Gögele, Maria Paulina Castelo-Rueda, Max Borsche, Irene Pichler, Christine Klein, Meike Kasten, Cleo Kritzinger, Clemens Egger, Norbert Brüggemann, Peter P. Pramstaller, Deborah Mascalzoni, Jannik Prasuhn, Andrew A. Hicks, Lynn Langlott
Publikováno v:
Parkinsonism & Related Disorders. 86:101-104
Background Heterozygous carriers of Parkin mutations are suggested to be at risk of developing Parkinson's disease, while biallelic variants are associated with typical autosomal recessive early-onset PD. Investigating unaffected heterozygous mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1070b6914d47367d587f793d0b6bd62
https://doi.org/10.1016/j.parkreldis.2021.03.028
https://doi.org/10.1016/j.parkreldis.2021.03.028
