Gadalla et al., 2011 - Google Patents
MeCP2 and Rett syndrome: reversibility and potential avenues for therapyGadalla et al., 2011
View PDF- Document ID
- 990560087871002759
- Author
- Gadalla K
- Bailey M
- Cobb S
- Publication year
- Publication venue
- Biochemical Journal
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Snippet
Mutations in the X-linked gene MECP2 (methyl CpG-binding protein 2) are the primary cause of the neurodevelopmental disorder RTT (Rett syndrome), and are also implicated in other neurological conditions. The expression product of this gene, MeCP2, is a widely …
- 102100014726 MECP2 0 title abstract description 389
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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