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Noncoding RET variants explain the strong association with ..:
Virtanen, Valtter B.
;
Salo, Perttu P.
;
Cao, Jia
...
European Journal of Medical Genetics. 62 (2019) 4 - p. 229-234 , 2019
Link:
https://doi.org/10.1016/j.ejmg.2018.07.019
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=cr-10.1016_j.ejmg.2018.07.019&Exemplar=1&LAN=DE A1 Virtanen, Valtter B. A1 Salo, Perttu P. A1 Cao, Jia A1 Löf-Granström, Anna A1 Milani, Lili 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 BV YR 2019 SN 1769-7212 JF European Journal of Medical Genetics VO 62 IS 4 SP 229 OP 234 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2018.07.019 DO https://doi.org/10.1016/j.ejmg.2018.07.019 SF ELIB - SuUB Bremen
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