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pro vyhledávání: '"Fiona Bonello"'
Autor:
Suzanne Lesage, Philip M Beart, Adeline Muscat, Fiona Bonello, Sidi-Mohamed Hassoun, Alexis Brice, Olga Corti, François Mouton-Liger, Jean-Christophe Corvol, Christelle Tesson, Yea Seul Shin, Johannes Krupp
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2019, 28 (10), pp.1645-1660. ⟨10.1093/hmg/ddz004⟩
Human Molecular Genetics, 2019, 28 (10), pp.1645-1660. ⟨10.1093/hmg/ddz004⟩
Human Molecular Genetics, Oxford University Press (OUP), 2019, 28 (10), pp.1645-1660. ⟨10.1093/hmg/ddz004⟩
Human Molecular Genetics, 2019, 28 (10), pp.1645-1660. ⟨10.1093/hmg/ddz004⟩
International audience; Mutations of LRRK2, encoding leucine-rich repeat kinase 2 (LRRK2), are the leading cause of autosomal dominant Parkinson's disease (PD). The most frequent of these mutations, G2019S substitution, increases kinase activity, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::140e626bb367ccae096121aa8242812d
https://hal.sorbonne-universite.fr/hal-02408164
https://hal.sorbonne-universite.fr/hal-02408164