Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

Daniella Magen, Ayala Ofir, Liron Berger, Dorit Goldsher, Ayelet Eran, Nassser Katib, Yousif Nijem, Euvgeni Vlodavsky, Shay Zur, Doron M. Behar,

Human Genetics · 2015 · 73 citations · 27 references

Concepts

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