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Noncoding RET variants explain the strong association with ..:
Virtanen, Valtter B
;
Salo, Perttu P
;
Gao, Jia
...
10.1016/j.ejmg.2018.07.019. , 2020
Link:
http://hdl.handle.net/10138/314531
RT Journal T1
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_314531&Exemplar=1&LAN=DE A1 Virtanen, Valtter B A1 Salo, Perttu P A1 Gao, Jia A1 Löf-Granström, Anna A1 Milani, Lill A1 Metspalu, Andres A1 Rintala, Risto J A1 Saarenpää-Heikkilä, Outi A1 Paunio, Tiina A1 Wester, Tomas A1 Nordenskjöld, Agneta A1 Perola, Markus A1 Pakarinen, Mikko P PB Elsevier Scientific Publ. Co YR 2020 K1 Hirschsprung disease K1 RET K1 Genetics K1 GWAS K1 NERVOUS-SYSTEM DEVELOPMENT K1 MUTATIONS K1 GENE K1 EXPRESSION K1 developmental biology K1 physiology K1 Biomedicine JF 10.1016/j.ejmg.2018.07.019 LK http://hdl.handle.net/10138/314531 DO http://hdl.handle.net/10138/314531 SF ELIB - SuUB Bremen
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