SnapShot: FMRP interacting proteins.
Cell
; 159(1): 218-218.e1, 2014 Sep 25.
Article
em En
| MEDLINE
| ID: mdl-25259928
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.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Proteína do X Frágil da Deficiência Intelectual
Limite:
Animals
/
Humans
Idioma:
En
Ano de publicação:
2014
Tipo de documento:
Article