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Mutational Analysis of Methyl‐CpG Binding Protein 2 (MECP2) Gene in Indian Cases of Rett Syndrome
Rett syndrome (RTT) is an X‐linked postnatal neurological disorder, primarily affecting females and characterized by regression, epilepsy, stereotypical hand movements, and motor abnormalities. Its prevalence is about 1 in 10,000 female births. RTT is caused by mutations within methyl CpG‐binding pr...
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| Publicado no: | J Clin Lab Anal |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807519/ https://ncbi.nlm.nih.gov/pubmed/23400946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21574 |
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