Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients
<p>Abstract</p> <p>Background</p> <p>More than 85% of Rett syndrome (RTT) patients have heterozygous mutations in the X-linked <it>MECP2 </it>gene which encodes methyl-CpG-binding protein 2, a transcriptional repressor that binds methylated CpG sites. Becaus...
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Format: | Book |
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BMC,
2006-07-01T00:00:00Z.
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A1234.567 |
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