correction to lancet diabetes endocrinol 2013; published online sept 6

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Corrections www.thelancet.com/diabetes-endocrinology Vol 1 November 2013 e14 Correction to Lancet Diabetes Endocrinol 2013; published online Sept 6 Busiah K, Drunat S, Vaivre-Douret L, et al, on behalf of the French NDM study group. Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study. Lancet Diabetes Endocrinol 2013; published online Sept 6. http://dx.doi.org/10.1016/ S2213-8587(13)70059-7—The title of this Article should have been “Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study”. Also, in the last paragraph of the Results, the proportions of index patients who had remission before age 1 year was 34 of 35 (97%) for patients with 6q24 abnormalities versus 20 of 71 (28%) patients with mutations in K ATP channel genes. These corrections have been made to the online version as of Oct 10, 2013, and the printed Article will be correct. Published Online October 10, 2013 http://dx.doi.org/10.1016/ S2213-8587(13)70115-3

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Corrections

www.thelancet.com/diabetes-endocrinology Vol 1 November 2013 e14

Correction to Lancet Diabetes Endocrinol 2013; published online Sept 6Busiah K, Drunat S, Vaivre-Douret L, et al, on behalf of the French NDM study group. Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study. Lancet Diabetes Endocrinol 2013; published online Sept 6. http://dx.doi.org/10.1016/S2213-8587(13)70059-7—The title of this Article should have been “Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study”. Also, in the last paragraph of the Results, the proportions of index patients who had remission before age 1 year was 34 of 35 (97%) for patients with 6q24 abnormalities versus 20 of 71 (28%) patients with mutations in KATP

channel genes. These corrections have been made to the online version as of Oct 10, 2013, and the printed Article will be correct.

Published OnlineOctober 10, 2013http://dx.doi.org/10.1016/S2213-8587(13)70115-3