Sequence 1 from Patent EP2430038

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APOE3 Christchurch Heterozygosity and Autosomal Dominant Alzheimer's Disease. [N Engl J Med. 2024]
APOE3 Christchurch Heterozygosity and Autosomal Dominant Alzheimer's Disease.
Quiroz YT, Aguillon D, Aguirre-Acevedo DC, Vasquez D, Zuluaga Y, Baena AY, Madrigal L, Hincapié L, Sanchez JS, Langella S, et al. N Engl J Med. 2024 Jun 20; 390(23):2156-2164.
Presenilin-1 ΔE9 mutation associated sarcoplasmic reticulum leak alters [Ca(2+)](i) distribution in human iPSC-derived cardiomyocytes. [J Mol Cell Cardiol. 2024]
Presenilin-1 ΔE9 mutation associated sarcoplasmic reticulum leak alters [Ca(2+)](i) distribution in human iPSC-derived cardiomyocytes.
Naumenko N, Koivumäki JT, Lunko O, Tuomainen T, Leigh R, Rabiee M, Laurila J, Oksanen M, Lehtonen S, Koistinaho J, et al. J Mol Cell Cardiol. 2024 Aug; 193:78-87. Epub 2024 Jun 6.
The presenilin 1 mutation P436S causes familial Alzheimer's disease with elevated Aβ43 and atypical clinical manifestations. [Alzheimers Dement. 2024]
The presenilin 1 mutation P436S causes familial Alzheimer's disease with elevated Aβ43 and atypical clinical manifestations.
Arber C, Belder CRS, Tomczuk F, Gabriele R, Buhidma Y, Farrell C, O'Connor A, Rice H, Lashley T, Fox NC, et al. Alzheimers Dement. 2024 Jul; 20(7):4717-4726. Epub 2024 Jun 2.

RefSeq alternative splicing
See 18 reference mRNA sequence splice variants for the PSEN1 gene.

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Nucleotide