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Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.

Bibliographic reference Ostergaard, Pia ; Simpson, Michael A ; Mendola, Antonella ; Vasudevan, Pradeep ; Connell, Fiona C ; et. al. Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.. In: American journal of human genetics, Vol. 90, no.2, p. 356-62 (2012)
Permanent URL http://hdl.handle.net/2078.1/120166