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eNauka >  Results >  Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease Role of a single hit?
Title: Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease Role of a single hit?
Authors: Hedrich, Katja; Hagenah, Johann M; Djarmati, Ana; Hiller, A; Lohnau, T; Lasek, K; Grunewald, RA; Hilker, R; Steinlechner, S; Boston, H;
Kock, Norman; Schneider-Gold, C; Kress, W; Siebner, Hartwig R; Binkofski, Ferdinand; Lencer, R; Munchau, A; Klein, Christine;
Issue Date: 2006
Publication: ARCHIVES OF NEUROLOGY
ISSN: 0003-9942 Archives of Neurology Search Idenfier
Type: Article
Collation: vol. 63 br. 6 str. 833-833
DOI: 10.1001/archneur.63.6.833
WoS-ID: 000238197600006
Scopus-ID: 2-s2.0-33745099053
URI: https://enauka.gov.rs/handle/123456789/797760
Metadata source: (Preuzeto iz Nasi u WoS)
M-category: 
21aM21a

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