DOI: 10.1055/s-00000071

Seminars in Neurology

References

Bassuk AG, Wallace RH, Buhr A , et al.
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.

Am J Hum Genet 2008;
83 (5) 572-581

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