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
2014-01-01
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.File in questo prodotto:
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