Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort

Cacace, R (author)

Van den Bossche, T (author)

Engelborghs, S (author)

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Geerts, N (author)

Laureys, A (author)

Dillen, L (author)

Graff, C (author)

Karolinska Institutet

Thonberg, H (author)

Karolinska Institutet

Chiang, HH (author)

Pastor, P (author)

Ortega-Cubero, S (author)

Pastor, MA (author)

Diehl-Schmid, J (author)

Alexopoulos, P (author)

Benussi, L (author)

Ghidoni, R (author)

Binetti, G (author)

Nacmias, B (author)

Sorbi, S (author)

Sanchez-Valle, R (author)

Llado, A (author)

Gelpi, E (author)

Almeida, MR (author)

Santana, I (author)

Tsolaki, M (author)

Koutroumani, M (author)

Clarimon, J (author)

Lleo, A (author)

Fortea, J (author)

de Mendonca, A (author)

Martins, M (author)

Borroni, B (author)

Padovani, A (author)

Matej, R (author)

Rohan, Z (author)

Vandenbulcke, M (author)

Vandenberghe, R (author)

De Deyn, PP (author)

Cras, P (author)

van der Zee, J (author)

Sleegers, K (author)

Van Broeckhoven, C (author)

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 (creator_code:org_t)

2015-10-14

2015

English.

In: Human mutation. - : Hindawi Limited. - 1098-1004 .- 1059-7794. ; 36:12, s. 1226-1235

Related links:

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https://doi.org/10.1...

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• Journal article (peer-reviewed)