Deletions in CCM2 Are a Common Cause of Cerebral Cavernous Malformations

The American Journal of Human Genetics - Tập 80 - Trang 69-75 - 2007
Christina L. Liquori1, Michel J. Berg2, Ferdinando Squitieri3, Tracey P. Leedom, Louis Ptacek4, Eric W. Johnson5, Douglas A. Marchuk1
1Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC (C.L.L.; T.P.L; D.A.M.)
2Strong Epilepsy Center, Department of Neurology, University of Rochester Medical Center, Rochester, NY (M.J.B.)
3Italy (F.S.)
4Department of Neurology, Howard Hughes Medical Institute, University of California–San Francisco, San Francisco (L.P.)
5Molecular Diagnostics and Biobanking, Prevention Genetics, Marshfield, WI (E.W.J.)

Tài liệu tham khảo

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