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MECP2 Duplication Syndrome

Since the initial report that clearly established a causal role between duplication of the MECP2 gene and a severe syndromic form of intellectual disability, many new patients have been identified and reported, and the etiology in already published families solved. This has led to the establishment...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखक: Van Esch, H.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: S. Karger AG 2012
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3366699/
https://ncbi.nlm.nih.gov/pubmed/22679399
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000329580
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