Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

BACKGROUND: Rett syndrome (RTT), a common cause of mental retardation in girls, is associated with mutations in the MECP2 gene. Most human cases of MECP2 mutation in girls result in classical or variant forms of RTT. When these same mutations occur in males, they often present as severe neonatal enc...

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Bibliografiske detaljer
Main Authors: Jentarra, Garilyn M, Olfers, Shannon L, Rice, Stephen G, Srivastava, Nishit, Homanics, Gregg E, Blue, Mary, Naidu, SakkuBai, Narayanan, Vinodh
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2010
Fag:
Research article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2836362/
https://ncbi.nlm.nih.gov/pubmed/20163734
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2202-11-19
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