A point mutation in KINDLIN3 ablates activation of three integrin subfamilies in humans.
Malinin NL; Zhang L; Choi J; Ciocea A; Razorenova O; Ma YQ; Podrez EA; Tosi M; Lennon DP; Caplan AI; Shurin SB; Plow EF; Byzova TV; Nature Medicine, 2009, vol. 15, issue 3, p 313, ISSN 1546170x. ISBN 1546170x.

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