The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.

Pasciuto, E., & Bagni, C. (2014). SnapShot: FMRP interacting proteins. CELL, 159(1), 218-218.e1 [10.1016/j.cell.2014.08.036].

SnapShot: FMRP interacting proteins

BAGNI, CLAUDIA
2014

Abstract

The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/13
English
Animals; Fragile X Mental Retardation Protein; Fragile X Syndrome; Humans; Protein Interaction Maps; RNA, Messenger
Pasciuto, E., & Bagni, C. (2014). SnapShot: FMRP interacting proteins. CELL, 159(1), 218-218.e1 [10.1016/j.cell.2014.08.036].
Pasciuto, E; Bagni, C
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2108/136333
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