(Q27654191)

English

Molecular Basis of Filamin A-FilGAP Interaction and Its Impairment in Congenital Disorders Associated with Filamin A Mutations

scientific article

  • Molecular basis of filamin A-FilGAP interaction and its impairment in congenital disorders associated with filamin A mutations

Statements

Molecular Basis of Filamin A-FilGAP Interaction and Its Impairment in Congenital Disorders Associated with Filamin A Mutations (English)
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Fumihiko Nakamura
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Outi Heikkinen
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Teresia M Osborn
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David A Weitz
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Olga Kupiainen
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John H Hartwig
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Thomas P Stossel
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2009
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4
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e4928
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