Open AccessCorrection: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth
Author(s) -
Johanna M. Huusko,
Minna K. Karjalainen,
Britney E. Graham,
Ge Zhang,
Emily Farrow,
Neil Miller,
Bo Jacobsson,
Haley Eidem,
Jeffrey C. Murray,
Bruce Bedell,
Patrick Breheny,
Noah W. Brown,
Frans L. Bødker,
Nadia K. Litterman,
Panpan Jiang,
Lauren Russell,
David A. Hinds,
Youna Hu,
Antonis Rokas,
Kari Teramo,
Kaare Christensen,
Scott M. Williams,
Mika Rämet,
Stephen F. Kingsmore,
Kelli K. Ryckman,
Mikko Hallman,
Louis J. Muglia
Publication year - 2018
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/journal.pgen.1007673
Subject(s) - biology , exome sequencing , exome , genetics , computational biology , bioinformatics , mutation , gene