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Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant
Virtanen, Valtter B., Salo, Perttu P., Cao, Jia, Löf-Granström, Anna, Milani, Lili, Metspalu, Andres, Rintala, Risto J., Saarenpää-Heikkilä, Outi, Paunio, Tiina, Wester, Tomas, Nordenskjöld, Agneta, PLanguage:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2018.07.019
Date:
July, 2018
File:
PDF, 803 KB
english, 2018