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Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy
P. Ostergaard, M.A. Simpson, A. Mendola, P. Vasudevan, F.C. Connell, A. van Impel, A.T. Moore, B.L. Loeys, A. Ghalamkarpour, A. Onoufriadis, I. Martinez-Corral, S. Devery, J.G. Leroy, L. van Laer, A. Singer, M.G. Bialer, M. McEntagart, O. Quarrell, G. Brice, R.C. Trembath
Research output: Contribution to journal/periodical › Article › Scientific › peer-review
136
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