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Details on Person Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome
| Class:Id | LiteratureReference:9022587 |
|---|---|
| _displayName | Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome |
| _timestamp | 2017-09-25 13:48:37 |
| author | [Person:9022552] Yasui, Dag H [Person:9022586] Gonzales, Michael L [Person:9022581] Aflatooni, Justin O [Person:9022580] Crary, Florence K [Person:9022583] Hu, Daniel J [Person:9022582] Gavino, Bryant J [Person:9022585] Golub, Mari S [Person:4839783] Vincent, John B [Person:9022579] Carolyn Schanen, N [Person:9022570] Olson, Carl O [Person:5619461] Rastegar, Mojgan [Person:9020655] LaSalle, Janine M |
| created | [InstanceEdit:9022584] Orlic-Milacic, Marija, 2017-09-25 |
| journal | Hum. Mol. Genet. |
| pages | 2447-58 |
| pubMedIdentifier | 24352790 |
| title | Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome |
| volume | 23 |
| year | 2014 |
| (literatureReference) | [Pathway:8986944] Transcriptional Regulation by MECP2 [Homo sapiens] |
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No pathways have been reviewed or authored by Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome (9022587)
