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MECP2 Mutations in People without Rett Syndrome
Mutations in Methyl-CpG-Binding protein 2 (MECP2) are commonly associated with and the neurodevelopmental disorder Rett syndrome (RTT). However, some people with RTT do not have mutations in MECP2, and interestingly there have been people identified with MECP2 mutations that do not have the clinical...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3880396/ https://ncbi.nlm.nih.gov/pubmed/23921973 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10803-013-1902-z |
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