MECP2 Mutation Interrupts Nucleolin-mTOR-P70S6K Signaling in Rett Syndrome Patients

Olson, CO; Pejhan, S; Kroft, D; Sheikholeslami, K; Fuss, D; Buist, M; Sher, AA; Del Bigio, MR; Sztainberg, Y; Sius, VM; Ang, LC; Sabourin-Felix, M; Moss, T; Rastegar, M

Rastegar, M (reprint author), Univ Manitoba, Regenerat Med Program, Max Rady Coll Med, Rady Fac Hlth Sci, Winnipeg, MB, Canada.; Rastegar, M (reprint author), Univ Manitoba, Dept Biochem & Med Genet, Max Rady Coll Med, Rady Fac Hlth Sci, Winnipeg, MB, Can

FRONTIERS IN GENETICS, 2018; 9 ():

Abstract

Rett syndrome (RTT) is a severe and rare neurological disorder that is caused by mutations in the X-linked MECP2 (methyl CpG-binding protein 2) gene. ......

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