Association between HFE 187 C>G (H63D) mutation and early-onset familial Alzheimer’s disease PSEN-1 839A>C (E280A) mutation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00277-008-0467-y.pdf
Reference8 articles.
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2. Arcos-Burgos M, Muenke M (2002) Genetics of population isolates. Clin Genet 61:233–247
3. Smith MA, Harris PL, Sayre LM, Perry G (1997) Iron accumulation in Alzheimer disease is a source of redox-generated free radicals. Proc Natl Acad Sci U S A 94:9866–9868
4. Connor JR, Milward EA, Moalem S, Sampietro M, Boyer P, Percy ME, Vergani C, Scott RJ, Chorney M (2001) Is hemochromatosis a risk factor for Alzheimer’s disease? J Alzheimer’s Dis 3:471–477
5. Sampietro M, Caputo L, Casatta A, Meregalli M, Pellagatti A, Tagliabue J, Annoni G, Vergani C (2001) The hemochromatosis gene affects the age of onset of sporadic Alzheimer’s disease. Neurobiol Aging 22:563–568
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1. The roles of iron and HFE genotype in neurological diseases;Molecular Aspects of Medicine;2020-10
2. LSD1 coordinates with the SIN3A/HDAC complex and maintains sensitivity to chemotherapy in breast cancer;Journal of Molecular Cell Biology;2018-05-08
3. Phenotypic Profile of Early-Onset Familial Alzheimer's Disease Caused by Presenilin-1 E280A Mutation;Journal of Alzheimer's Disease;2012-09-25
4. HFE Gene Variants Affect Iron in the Brain;The Journal of Nutrition;2011-02-23
5. The H63D HFE gene variant promotes activation of the intrinsic apoptotic pathway via mitochondria dysfunction following β-amyloid peptide exposure;Journal of Neuroscience Research;2010-08-23
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