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Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism

✍ Scribed by Plank, Sara M. ;Copeland-Yates, Susan A. ;Sossey-Alaoui, Khalid ;Bell, Jennifer M. ;Schroer, Richard J. ;Skinner, Cindy ;Michaelis, Ron C.


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
68 KB
Volume
105
Category
Article
ISSN
0148-7299

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Inheritance of the apolipoprotein E E 4 allele is a risk factor for Alzheimer's disease (AD). A recent report studying Japanese patients suggested that a polymorphism of a trinucleotide repeat in the 5' untranslated region of an apolipoprotein E receptor, the very-low-density lipoprotein receptor, i