(Q27654191)
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
e4928
0 references
3
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