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Volumn 12, Issue 10, 2016, Pages

Erratum: Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer’s Disease (PLoS Genetics (2016) 12:10 (e1006327) DOI: 10.1371/journal.pgen.1006327);Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

(52)  Jakobsdottir, Johanna a   van der Lee, Sven J b   Bis, Joshua C c   Chouraki, Vincent d,e   Li Kroeger, David f,g   Yamamoto, Shinya f,g   Grove, Megan L h   Naj, Adam i   Vronskaya, Maria j   Salazar, Jose L f   DeStefano, Anita L e,k   Brody, Jennifer A c   Smith, Albert V a,l   Amin, Najaf b   Sims, Rebecca j   Ibrahim Verbaas, Carla A b   Choi, Seung Hoan e,k   Satizabal, Claudia L d,e   Lopez, Oscar L m   Beiser, Alexa d,e,k   more..


Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID BETA PROTEIN; APOLIPOPROTEIN E; MEMBRANE PROTEIN; NOTCH RECEPTOR; PRESENILIN; PROTEIN SKAP2; PROTEIN TM2D3; UNCLASSIFIED DRUG; AMX PROTEIN, DROSOPHILA; AMYLOID PRECURSOR PROTEIN; APOE PROTEIN, HUMAN; DROSOPHILA PROTEIN; SIGNAL PEPTIDE; SRC KINASE ASSOCIATED PHOSPHOPROTEIN 2; TM2D1 PROTEIN, HUMAN; TROPOMYOSIN;

EID: 84994310331     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/JOURNAL.PGEN.1006456     Document Type: Erratum
Times cited : (44)

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