Abstract
British Journal of Hospital MedicineVol. 74, No. 2 Clinical NewsGenetic sequencing breakthrough to aid treatment for congenital hyperinsulinismSian EllardSian EllardSearch for more papers by this authorSian EllardPublished Online:27 Sep 2013https://doi.org/10.12968/hmed.2013.74.2.68AboutSectionsView articleView Full TextPDF/EPUB ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareShare onFacebookTwitterLinked InEmail View article References Flanagan SE, Xie W, Caswell R et al. (2013) Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation. Am J Hum Genet 92(1): 131–6 Crossref, Medline, Google Scholar FiguresReferencesRelatedDetails 1 February 2013Volume 74Issue 2ISSN (print): 1750-8460ISSN (online): 1759-7390 Metrics History Published online 27 September 2013 Published in print 1 February 2013 Information© MA Healthcare LimitedPDF download
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