Editorial comment on “Whole Exome Sequencing Identifies Compound Heterozygous Mutations in WDR62 in Siblings With Recurrent Polymicrogyria”

Abstract

American Journal of Medical Genetics Part AVolume 155, Issue 9 p. 2069-2070 Invited Comment Editorial comment on “Whole Exome Sequencing Identifies Compound Heterozygous Mutations in WDR62 in Siblings With Recurrent Polymicrogyria”† Leslie G. Biesecker, Corresponding Author Leslie G. Biesecker lesb@mindspring.com Deputy Editor, American Journal of Medical Genetics, Bethesda, MarylandDeputy Editor, American Journal of Medical Genetics, 5523 Oakmont Ave, Bethesda, MD 20817.Search for more papers by this author Leslie G. Biesecker, Corresponding Author Leslie G. Biesecker lesb@mindspring.com Deputy Editor, American Journal of Medical Genetics, Bethesda, MarylandDeputy Editor, American Journal of Medical Genetics, 5523 Oakmont Ave, Bethesda, MD 20817.Search for more papers by this author First published: 10 August 2011 https://doi.org/10.1002/ajmg.a.34183Citations: 6 † How to Cite this Article: Biesecker LG. 2011. Editorial comment on “Whole Exome Sequencing Identifies Compound Heterozygous Mutations in WDR62 in Siblings With Recurrent Polymicrogyria”. Am J Med Genet Part A 155:2069–2070. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume155, Issue9September 2011Pages 2069-2070 RelatedInformation