CSTB null mutation associated with microcephaly, early developmental delay, and severe dyskinesia.
Mancini GM, Schot R, de Wit MC, de Coo RF, Oostenbrink R, Bindels-de Heus K, Berger LP, Lequin MH, de Vries FA, Wilke M, van Slegtenhorst MA.
Mancini GM, et al. Among authors: de vries fa, de wit mc, de coo rf.
Neurology. 2016 Mar 1;86(9):877-8. doi: 10.1212/WNL.0000000000002422. Epub 2016 Feb 3.
Neurology. 2016.
PMID: 26843564
No abstract available.