DLX5 and DLX6 Expression Is Biallelic and Not Modulated by MeCP2 Deficiency
The American Journal of Human Genetics2007Vol. 81(3), pp. 492–506
Citations Over TimeTop 10% of 2007 papers
Related Papers
- → A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome(2001)1,559 cited
- → Rett Syndrome and MeCP2: Linking Epigenetics and Neuronal Function(2002)199 cited
- → MeCP2 Dysfunction in Humans and Mice(2005)90 cited
- → Ocular MECP2 Protein Expression in Patients With and Without Rett Syndrome(2010)17 cited
- → Can we relate MeCP2 deficiency to the structural and chemical abnormalities in the Rett brain?(2005)18 cited