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Comment
. 2009 May-Jun;9(3):82-4.
doi: 10.1111/j.1535-7511.2009.01300.x.

A new, progressive myoclonic epilepsy: is it a chronicle of the noncanonical or a failure to REST?

Martin Gallagher
Comment

A new, progressive myoclonic epilepsy: is it a chronicle of the noncanonical or a failure to REST?

Martin Gallagher. Epilepsy Curr. 2009 May-Jun.
No abstract available

PubMed Disclaimer

Comment on

  • A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
    Bassuk AG, Wallace RH, Buhr A, Buller AR, Afawi Z, Shimojo M, Miyata S, Chen S, Gonzalez-Alegre P, Griesbach HL, Wu S, Nashelsky M, Vladar EK, Antic D, Ferguson PJ, Cirak S, Voit T, Scott MP, Axelrod JD, Gurnett C, Daoud AS, Kivity S, Neufeld MY, Mazarib A, Straussberg R, Walid S, Korczyn AD, Slusarski DC, Berkovic SF, El-Shanti HI. Bassuk AG, et al. Am J Hum Genet. 2008 Nov;83(5):572-81. doi: 10.1016/j.ajhg.2008.10.003. Epub 2008 Oct 30. Am J Hum Genet. 2008. PMID: 18976727 Free PMC article.

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