000 01090 a2200289 4500
005 20250515023824.0
264 0 _c20060801
008 200608s 0 0 eng d
022 _a0959-437X
024 7 _a10.1016/j.gde.2006.04.009
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMoretti, Paolo
245 0 0 _aMeCP2 dysfunction in Rett syndrome and related disorders.
_h[electronic resource]
260 _bCurrent opinion in genetics & development
_cJun 2006
300 _a276-81 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
650 0 4 _aAnimals
650 0 4 _aDisease Models, Animal
650 0 4 _aHumans
650 0 4 _aMethyl-CpG-Binding Protein 2
_xgenetics
650 0 4 _aMutation
_xgenetics
650 0 4 _aPhenotype
650 0 4 _aRett Syndrome
_xclassification
700 1 _aZoghbi, Huda Y
773 0 _tCurrent opinion in genetics & development
_gvol. 16
_gno. 3
_gp. 276-81
856 4 0 _uhttps://doi.org/10.1016/j.gde.2006.04.009
_zAvailable from publisher's website
999 _c16250226
_d16250226