Nature Genetics 38, 682 - 687 (2006)
Published online: 21 May 2006; | doi:10.1038/ng1802
Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidismValérie Senée, Claude Chelala, Sabine Duchatelet, Daorong Feng, Hervé Blanc, Jack-Christophe Cossec, Céline Charon, Marc Nicolino, Pascal Boileau, Douglas R Cavener, Pierre Bougnères, Doris Taha
& Cécile Julier Supplementary Fig. 1 (pdf 40K)
Mutation in a patient from family NDH1. Supplementary Fig. 2 (pdf 44K)
Human GLIS3 gene structure: alternative transcripts and predicted proteins. Supplementary Figure 3 (pdf 84K)
Facial features of patients NDH3-3 and NDH3-4 at ages 6 months and 2 years, respectively, showing characteristic facial morphology. Supplementary Table 1 (pdf 52K)
Biochemical characteristics of patients. Supplementary Table 2 (pdf 108K)
Primer sequences and PCR assays. Supplementary Table 3 (pdf 64K)
Exon-intron structure of the human GLIS3 gene. Supplementary Note (pdf 84K)
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