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- Sherrington, R (author)
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant
- Article/chapterEnglish1996
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- Oxford University Press (OUP),1996
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:1932900
- http://kipublications.ki.se/Default.aspx?queryparsed=id:1932900URI
- https://doi.org/10.1093/hmg/5.7.985DOI
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- Language:English
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- Froelich, S (author)
- Sorbi, S (author)
- Campion, D (author)
- Chi, H (author)
- Rogaeva, EA (author)
- Levesque, G (author)
- Rogaev, EI (author)
- Lin, C (author)
- Liang, Y (author)
- Ikeda, M (author)
- Mar, L (author)
- Brice, A (author)
- Agid, Y (author)
- Percy, ME (author)
- ClergetDarpoux, F (author)
- Piacentini, S (author)
- Marcon, G (author)
- Nacmias, B (author)
- Amaducci, L (author)
- Frebourg, T (author)
- Lannfelt, L (author)
- Rommens, JM (author)
- StGeorgeHyslop, PH (author)
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- In:Human molecular genetics: Oxford University Press (OUP)5:7, s. 985-9880964-69061460-2083
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