Molecular Basis of Filamin A-FilGAP Interaction and Its Impairment in Congenital Disorders Associated with Filamin A Mutations (Q27654191)
Jump to navigation
Jump to search
scientific article
- Molecular basis of filamin A-FilGAP interaction and its impairment in congenital disorders associated with filamin A mutations
Language | Label | Description | Also known as |
---|---|---|---|
English | Molecular Basis of Filamin A-FilGAP Interaction and Its Impairment in Congenital Disorders Associated with Filamin A Mutations |
scientific article |
|
Statements
Molecular Basis of Filamin A-FilGAP Interaction and Its Impairment in Congenital Disorders Associated with Filamin A Mutations (English)
0 references
2009
0 references
4
0 references
3
0 references
e4928
0 references
18 March 2009
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference