Molecular basis of filamin A-FilGAP interaction and its impairment in congenital disorders associated with filamin A mutations. oleh Fumihiko Nakamura, Outi Heikkinen, Olli T Pentikäinen, Teresia M Osborn, Karen E Kasza, David A Weitz, Olga Kupiainen, Perttu Permi, Ilkka Kilpeläinen, Jari Ylänne, John H Hartwig, Thomas P Stossel