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The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome
Rett syndrome (RTT) is a rare, severe disorder of neuronal plasticity that predominantly affects girls. Girls with RTT usually appear asymptomatic in the first 6–18 months of life, but gradually develop severe motor, cognitive, and behavioral abnormalities that persist for life. A predominance of ne...
में बचाया:
में प्रकाशित: | Front Cell Neurosci |
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मुख्य लेखकों: | , |
स्वरूप: | Artigo |
भाषा: | Inglês |
प्रकाशित: |
Frontiers Media S.A.
2015
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विषय: | |
ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4500929/ https://ncbi.nlm.nih.gov/pubmed/26236194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2015.00266 |
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