المؤلفون: Ben-Shachar S; Tel Aviv Medical Center, The Genetic Institute, 6 Weizmann Street, 6423906, Tel Aviv, Israel. shayb@tlvmc.gov.il.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. shayb@tlvmc.gov.il., Afawi Z; Center for Neuroscience, Ben-Gurion University of the Negev, Be'er Sheva, Israel., Masalha R; Department of Neurology, Soroka Medical Center, Ben-Gurion University of the Negev, Be'er Sheva, Israel., Badarny S; Department of Neurology, Carmel Medical Center, Rappaport Faculty of Medicine - The Technion, Haifa, Israel., Neiman T; Tel Aviv Medical Center, The Genetic Institute, 6 Weizmann Street, 6423906, Tel Aviv, Israel., Pavzner D; Tel Aviv Medical Center, The Genetic Institute, 6 Weizmann Street, 6423906, Tel Aviv, Israel., Bar-Shira A; Tel Aviv Medical Center, The Genetic Institute, 6 Weizmann Street, 6423906, Tel Aviv, Israel., Orr-Urtreger A; Tel Aviv Medical Center, The Genetic Institute, 6 Weizmann Street, 6423906, Tel Aviv, Israel.; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

المصدر: Journal of molecular neuroscience : MN [J Mol Neurosci] 2017 Oct; Vol. 63 (2), pp. 216-222. Date of Electronic Publication: 2017 Sep 15.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Humana Press Country of Publication: United States NLM ID: 9002991 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1559-1166 (Electronic) Linking ISSN: 08958696 NLM ISO Abbreviation: J Mol Neurosci Subsets: MEDLINE

مواضيع طبية MeSH: Mutation*, Parkinson Disease/*genetics , Ubiquitin-Protein Ligases/*genetics, Adolescent ; Adult ; Age of Onset ; Female ; Heterozygote ; Homozygote ; Humans ; Male ; Parkinson Disease/pathology ; Pedigree