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An intronic mutation within FGB (IVS1+2076 ag) is associated with afibrinogenemia and recurrent transient ischemic attacks

Journal article published in 2006 by A. Dear, J. Daly ORCID, S. O. Brennan, A. Tuckfield, P. M. George
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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