Large-scale analysis of variation in the insulin-like growth factor family in humans reveals rare disease links and common polymorphisms. [Additions and Corrections]

VOLUME 292 (2017) PAGES 9252–9261PAGE 9254:There was an error in the text on page 9254, right column, second paragraph. “… most of this could be attributed to a single non-coding C to T change located 5′ to the adjacent INS gene (see single nucleotide polymorphism (SNP): rs14948363)” should be changed as follows. “… most of this could be attributed to a single non-coding C to T change located 3′ to the adjacent INS gene (see single nucleotide polymorphism (SNP): rs149483638).”

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