Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations
<p>Abstract</p> <p>Background</p> <p>Females with the neurological disorder Rett syndrome are heterozygous for mutations in X-linked MECP2 that encodes methyl-CpG binding protein 2 (MeCP2) thought to act as a transcriptional repressor. To identify target genes for MeCP2 modulation, we studied global...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2002-11-01
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| Col·lecció: | BMC Medical Genetics |
| Accés en línia: | http://www.biomedcentral.com/1471-2350/3/12 |
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