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Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

✍ Scribed by DZ Loesch; MS Khaniani; HR Slater; JP Rubio; QM Bui; K Kotschet; W D’Souza; A Venn; P Kalitsis; AKH Choo; T Burgess; L Johnson; A Evans; M Horne

Book ID
110888890
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
490 KB
Volume
76
Category
Article
ISSN
0009-9163

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Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles
✍ Brown, T. C.; Tarleton, J. C.; Go, R. C. P.; Longshore, J. W.; Descartes, M. 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 62 KB 👁 2 views

The fragile sites FRAXA and FRAXE, located ∼600 kb apart on Xq27.3 and Xq28, respectively, are due to a CGG trinucleotide repeat expansion. Although the expansion mechanism for these and other trinucleotide repeat disorders remains unknown, the similarities between the FRAXA and FRAXE regions sugges