Histone Modifications Depict an Aberrantly Heterochromatinized FMR1 Gene in Fragile X Syndrome
- 1 October 2002
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 71 (4) , 923-932
- https://doi.org/10.1086/342931
Abstract
No abstract availableKeywords
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