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Published in 2019 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms20205177
Abstract: The deletion of Mecp2, the gene encoding methyl-CpG-binding protein 2, causes severe breathing defects and developmental anomalies in mammals. In Mecp2-null mice, impaired GABAergic neurotransmission is demonstrated at the early stage of life. GABAergic dysfunction…
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Keywords:
null mice;
gad1 promoter;
mecp2;
mecp2 null ... See more keywords