Journal
Human Molecular Genetics
Publication Date
7-29-2020
Volume
29
Issue
12
First Page
2035
Last Page
2050
Document Type
Open Access Publication
DOI
10.1093/hmg/ddaa093
Rights and Permissions
Phoebe C R Parrish, Delong Liu, Russell H Knutsen, Charles J Billington, Jr, Robert P Mecham, Yi-Ping Fu, Beth A Kozel, Whole exome sequencing in patients with Williams–Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk, Human Molecular Genetics, Volume 29, Issue 12, 15 June 2020, Pages 2035–2050, https://doi.org/10.1093/hmg/ddaa093. Published by Oxford University Press 2020. This work is written by US Government employees and is in the public domain in the US.
Recommended Citation
Parrish, Phoebe C R; Liu, Delong; Knutsen, Russell H; Billington, Charles J; Mecham, Robert P; Fu, Yi-Ping; and Kozel, Beth A, "Whole exome sequencing in patients with Williams-Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk." Human Molecular Genetics. 29, 12. 2035 - 2050. (2020).
https://digitalcommons.wustl.edu/oa_4/940
Additional Links
Supplemental material is available for this article at publisher site.
