Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
Am J Hum Genet
.
2017 Dec 7;101(6):1034.
doi: 10.1016/j.ajhg.2017.11.003.
Authors
Simone Sanna-Cherchi
,
Kamal Khan
,
Rik Westland
,
Priya Krithivasan
,
Lorraine Fievet
,
Hila Milo Rasouly
,
Iuliana Ionita-Laza
,
Valentina P Capone
,
David A Fasel
,
Krzysztof Kiryluk
,
Sitharthan Kamalakaran
,
Monica Bodria
,
Edgar A Otto
,
Matthew G Sampson
,
Christopher E Gillies
,
Virginia Vega-Warner
,
Katarina Vukojevic
,
Igor Pediaditakis
,
Gabriel S Makar
,
Adele Mitrotti
,
Miguel Verbitsky
,
Jeremiah Martino
,
Qingxue Liu
,
Young-Ji Na
,
Vinicio Goj
,
Gianluigi Ardissino
,
Maddalena Gigante
,
Loreto Gesualdo
,
Magdalena Janezcko
,
Marcin Zaniew
,
Cathy Lee Mendelsohn
,
Shirlee Shril
,
Friedhelm Hildebrandt
,
Joanna A E van Wijk
,
Adela Arapovic
,
Marijan Saraga
,
Landino Allegri
,
Claudia Izzi
,
Francesco Scolari
,
Velibor Tasic
,
Gian Marco Ghiggeri
,
Anna Latos-Bielenska
,
Anna Materna-Kiryluk
,
Shrikant Mane
,
David B Goldstein
,
Richard P Lifton
,
Nicholas Katsanis
,
Erica E Davis
,
Ali G Gharavi
PMID:
29220675
PMCID:
PMC5812917
DOI:
10.1016/j.ajhg.2017.11.003
No abstract available
Publication types
Published Erratum
Grants and funding
P30 DK079310/DK/NIDDK NIH HHS/United States
S10 OD018521/OD/NIH HHS/United States
UL1 TR001863/TR/NCATS NIH HHS/United States