Whole genomes in the clinic: uncovering de novo mutations in sporadic infantile epilepsy

Clin Genet. 2012 Jul;82(1):28-9. doi: 10.1111/j.1399-0004.2012.01893.x. Epub 2012 May 17.

Author

C Kay¹

Affiliation

¹ Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, BC, Canada. ckay@cmmt.ubc.ca

PMID: 22537398
DOI: 10.1111/j.1399-0004.2012.01893.x

No abstract available

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