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

Autor: 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, Perola, Markus, Pakarinen, Mikko P.
Zdroj: In European Journal of Medical Genetics April 2019 62(4):229-234
Databáze: ScienceDirect
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