Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots
- 1 December 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (6) , 1520-1529
- https://doi.org/10.1086/302690
Abstract
No abstract availableKeywords
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