Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant.

Added 422 days ago (22.07.2018)
Authors: Virtanen VB, Salo PP, Cao J, Löf-Granström A, Milani L, Metspalu A, Rintala RJ, Saarenpää-Heikkilä O, Paunio T, Wester T, Nordenskjöld A, Perola M, Pakarinen MP
PubMed id: 30031151
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