Title : Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region.

Pub. Date : 2001 Jun

PMID : 11453972






4 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Illegitimate recombination resulting in deletion at a substantial proportion of the shared MECP2 sites is enhanced by repeated guanosine (G) DNA sequences in the antisense direction, consistent with reports at other gene loci that polypurine (multiple guanosine or adenosine (A)) basepairs enhance sequence deletion. Guanosine methyl-CpG binding protein 2 Homo sapiens
2 Illegitimate recombination resulting in deletion at a substantial proportion of the shared MECP2 sites is enhanced by repeated guanosine (G) DNA sequences in the antisense direction, consistent with reports at other gene loci that polypurine (multiple guanosine or adenosine (A)) basepairs enhance sequence deletion. polypurine methyl-CpG binding protein 2 Homo sapiens
3 Illegitimate recombination resulting in deletion at a substantial proportion of the shared MECP2 sites is enhanced by repeated guanosine (G) DNA sequences in the antisense direction, consistent with reports at other gene loci that polypurine (multiple guanosine or adenosine (A)) basepairs enhance sequence deletion. Guanosine methyl-CpG binding protein 2 Homo sapiens
4 Illegitimate recombination resulting in deletion at a substantial proportion of the shared MECP2 sites is enhanced by repeated guanosine (G) DNA sequences in the antisense direction, consistent with reports at other gene loci that polypurine (multiple guanosine or adenosine (A)) basepairs enhance sequence deletion. Adenosine methyl-CpG binding protein 2 Homo sapiens