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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 2
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2003 6
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2005 3
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Page 1
Hereditary ferritinopathy.
Vidal R, Delisle MB, Rascol O, Ghetti B. Vidal R, et al. J Neurol Sci. 2003 Mar 15;207(1-2):110-1. doi: 10.1016/s0022-510x(02)00435-5. J Neurol Sci. 2003. PMID: 12614943 Review. No abstract available.
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant.
Sherrington R, Froelich S, Sorbi S, Campion D, Chi H, Rogaeva EA, Levesque G, Rogaev EI, Lin C, Liang Y, Ikeda M, Mar L, Brice A, Agid Y, Percy ME, Clerget-Darpoux F, Piacentini S, Marcon G, Nacmias B, Amaducci L, Frebourg T, Lannfelt L, Rommens JM, St George-Hyslop PH. Sherrington R, et al. Hum Mol Genet. 1996 Jul;5(7):985-8. doi: 10.1093/hmg/5.7.985. Hum Mol Genet. 1996. PMID: 8817335
32 results