Combined association of Presenilin-1 and Apolipoprotein E polymorphisms with maternal meiosis II error in Down syndrome births
Author:
Affiliation:
1. Maulana Abul Kalam Azad University of Technology, India
2. University of Calcutta, India
3. University of Pittsburgh, USA; University of Pittsburgh, USA
4. University of Pittsburgh, USA
5. Anthropological Survey of India, India
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v40n3/1415-4757-gmb-1678-4685-GMB-2016-0138.pdf
Reference88 articles.
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2. Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: A report from the Atlanta and National Down Syndrome Projects;Allen EG;Hum Genet,2009
3. Expression of the cyclin-dependent kinase inhibitor p16 in Alzheimer's disease;Arendt T;Neuroreports,1996
4. Apolipoprotein E allele distribution in parents of Down's syndrome children;Avramopoulos D;Lancet,1996
5. No association between an intronic polymorphism in the presenilin-1 gene and Alzheimer disease in a German population;Bagli M;J Neurol Sci,1999
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3. Endosome Dysregulation in Down Syndrome: A Potential Contributor to Alzheimer Disease Pathology;Annals of Neurology;2021-02-25
4. The Significance of Apolipoprotein E Measurement in the Screening of Fetal Down Syndrome;Journal of Clinical Medicine;2020-12-10
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