Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophy

Authors

D. Zhi, University of Alabama - Birmingham
M. R. Irvin, University of Alabama - BirminghamFollow
C. C. Gu, Washington University School of Medicine in St. LouisFollow
A. J. Stoddard, Medical College of Wisconsin
R. Lorier, Medical College of Wisconsin
A. Matter, Medical College of Wisconsin
D. C. Rao, Washington University School of Medicine in St. Louis
V Srinivasasainagendra, University of Alabama - Birmingham
H. K. Tiwari, University of Alabama - Birmingham
A. Turner, Medical College of Wisconsin
U. Broeckel, Medical College of WisconsinFollow
D. K. Arnett, University of Alabama - BirminghamFollow

Journal

Frontiers in Genetics

Publication Date

2012

Volume

3

Inclusive Pages

92

Document Type

Open Access Publication

DOI

10.3389/fgene.2012.00092

Rights and Permissions

Zhi D, Irvin MR, Gu CC, Stoddard AJ, Lorier R, Matter A, Rao DC, Srinivasasainagendra V, Tiwari HK, Turner A, Broeckel U and Arnett DK (2012) Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophy. Front. Gene. 3:92. doi: 10.3389/fgene.2012.00092

Recommended Citation

Zhi, D.; Irvin, M. R.; Gu, C. C.; Stoddard, A. J.; Lorier, R.; Matter, A.; Rao, D. C.; Srinivasasainagendra, V; Tiwari, H. K.; Turner, A.; Broeckel, U.; and Arnett, D. K., "Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophy." Frontiers in Genetics. 3, 92. (2012).
https://digitalcommons.wustl.edu/open_access_pubs/2245