MeCP2 dysfunction in Rett syndrome and related disorders. [electronic resource]
- Current opinion in genetics & development Jun 2006
- 276-81 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
0959-437X
10.1016/j.gde.2006.04.009 doi
Animals Disease Models, Animal Humans Methyl-CpG-Binding Protein 2--genetics Mutation--genetics Phenotype Rett Syndrome--classification