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European Journal of Endocrinology|February 19, 2013
Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1Maik Welzel, Leyla Akin, Anja Büscher, et al.
Hormone Research in Paediatrics|March 24, 2025
SKIN-PEDIC: A Worldwide Assessment of Skin Problems in Children and Adolescents Using Diabetes DevicesAnna Korsgaard Berg, Stefano Passanisi, Thekla von dem Berge, et al.
Nature Communications|November 30, 2016
Increased DNA methylation variability in type 1 diabetes across three immune effector cell typesDirk S Paul, Andrew E Teschendorff, Mary A N Dang, et al.
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