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Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus
Document Type
Artikel
Author
Fadista, J; Lund, M; Skotte, L; Geller, F; Nandakumar, P; Chatterjee, S; Matsson, H; Granstrom, AL; Wester, T; Salo, P; Virtanen, V; Carstensen, L; Bybjerg-Grauholm, J; Hougaard, DM; Pakarinen, M; Perola, M; Nordenskjold, A; Chakravarti, A; Melbye, M; Feenstra, B
Source
European journal of human genetics : EJHG. 26(4):561-569
Subject
Medicin och hälsovetenskap
Language
English
English
ISSN
1476-5438

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