Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome.
- DOI
- 10.1016/j.xhgg.2023.100232
- Published
- 2023 Oct 12
- Container
- HGG advances
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1016/j.xhgg.2023.100232,
title = {Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome.},
author = {Blue EE and White JJ and Dush MK and Gordon WW and Wyatt BH and White P and Marvin CT and Helle E and Ojala T and Priest JR and Jenkins MM and Almli LM and Reefhuis J and Pangilinan F and Brody LC and McBride KL and Garg V and Shaw GM and Romitti PA and Nembhard WN and Browne ML and Werler MM and Kay DM and National Birth Defects Prevention Study and University of Washington Center for Mendelian Genomics and Mital S and Chong JX and Nascone-Yoder NM and Bamshad MJ},
year = {2023},
journal = {HGG advances},
doi = {10.1016/j.xhgg.2023.100232},
url = {https://doi.org/10.1016/j.xhgg.2023.100232}
}RIS
TY - JOUR TI - Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome. AU - Blue EE AU - White JJ AU - Dush MK AU - Gordon WW AU - Wyatt BH AU - White P AU - Marvin CT AU - Helle E AU - Ojala T AU - Priest JR AU - Jenkins MM AU - Almli LM AU - Reefhuis J AU - Pangilinan F AU - Brody LC AU - McBride KL AU - Garg V AU - Shaw GM AU - Romitti PA AU - Nembhard WN AU - Browne ML AU - Werler MM AU - Kay DM AU - National Birth Defects Prevention Study AU - University of Washington Center for Mendelian Genomics AU - Mital S AU - Chong JX AU - Nascone-Yoder NM AU - Bamshad MJ PY - 2023 JO - HGG advances DO - 10.1016/j.xhgg.2023.100232 UR - https://doi.org/10.1016/j.xhgg.2023.100232 ER -
APA
EE, B., JJ, W., MK, D., WW, G., BH, W., P, W., CT, M., E, H., T, O., JR, P., MM, J., LM, A., J, R., F, P., LC, B., KL, M., V, G., GM, S., PA, R., WN, N., ML, B., MM, W., DM, K., Study, N. B. D. P., Genomics, U. O. W. C. F. M., S, M., JX, C., NM, N., & MJ, B. (2023). Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome.. HGG advances. https://doi.org/10.1016/j.xhgg.2023.100232
Source records
- pubmed · retrieved 2026-09-26T07:37:45.127Z