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Published in 2019 at "Human Molecular Genetics"
DOI: 10.1093/hmg/ddy393
Abstract: Abstract Mutations in myocyte enhancer factor 2C (MEF2C), an important transcription factor in neurodevelopment, are associated with a Rettālike syndrome. Structural variants (SVs) upstream of MEF2C, which do not disrupt the gene itself, have also…
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Keywords:
mef2c;
network;
rett like;
neuronal enhancer ... See more keywords