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Enhanced Dense Core Granule Function and Adrenal Hypersecretion in a Mouse Model of Rett Syndrome: Mecp2 Null Adrenal Dysfunction

Rett Syndrome (RTT) is a progressive developmental disorder resulting from loss of function mutations in the gene encoding MeCP2 (methyl-CpG-binding protein 2), a transcription regulatory protein. The RTT phenotype is complex and includes severe cardiorespiratory abnormalities, dysautonomia and beha...

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Bibliografski detalji
Glavni autori: Ladas, Thomas, Chan, Shyue-An, Ogier, Michael, Smith, Corey, Katz, David M.
Format: Artigo
Jezik:Inglês
Izdano: 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2758854/
https://ncbi.nlm.nih.gov/pubmed/19674087
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1460-9568.2009.06858.x
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