Exome sequencing identifies novel rare variant association signals in the Cooperative Health Research in South Tyrol (CHRIS) study

Conference paper

Peer reviewed

European Journal of Human Genetics, Vol.27(Suppl. 2)

27, Nature Publishing Group: Open Access Hybrid Model Option B

31/10/2019

Handle:

https://hdl.handle.net/10863/12262

Abstract

In: 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, SWEDEN, JUN 15-18, 2019, Meeting Abstract: P18.78B, p. 1777

Title: Exome sequencing identifies novel rare variant association signals in the Cooperative Health Research in South Tyrol (CHRIS) study
Creators: DB Emmert
J Mitchell
E König
M Gögele
C Pattaro
PP Pramstaller
Christian Fuchsberger
Publication Details: European Journal of Human Genetics, Vol.27(Suppl. 2)
ISSN: 1018-4813
EISSN: 1476-5438
Series / Volume: 27
Publisher: Nature Publishing Group: Open Access Hybrid Model Option B
Identifiers: (EURAC)21577249
991005772369101241
Web of Science ID: JC5ID
Academic Unit: Institute for Biomedicine
Language: English
Resource Type: Conference paper
Local Fields: Scientific
Author Names String: Emmert DB, Mitchell J, König E, Gögele M, Pattaro C, Pramstaller PP, Fuchsberger C

20 Record Views