Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects

Jessica X. Chong, Matthew Carter Childers, Colby T. Marvin, Allison J. Marcello, Hernan Gonorazky, Lili-Naz Hazrati, James J. Dowling, Fatema Al Amrani, Yasemin Alanay, Yolanda Nieto, Miguel Á Marín Gabriel, Arthur S. Aylsworth, Kati J. Buckingham, Kathryn M. Shively, Olivia Sommers, Kailyn Anderson, Michael Regnier, Michael J. Bamshad

Open source

DOI
10.1016/j.xhgg.2023.100213
Published
2023-07
Container
Human Genetics and Genomics Advances
Publisher
Elsevier BV
Open access
unknown

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BibTeX

@article{allodium:10.1016/j.xhgg.2023.100213,
  title = {Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects},
  author = {Jessica X. Chong and Matthew Carter Childers and Colby T. Marvin and Allison J. Marcello and Hernan Gonorazky and Lili-Naz Hazrati and James J. Dowling and Fatema Al Amrani and Yasemin Alanay and Yolanda Nieto and Miguel Á Marín Gabriel and Arthur S. Aylsworth and Kati J. Buckingham and Kathryn M. Shively and Olivia Sommers and Kailyn Anderson and Michael Regnier and Michael J. Bamshad},
  year = {2023},
  journal = {Human Genetics and Genomics Advances},
  doi = {10.1016/j.xhgg.2023.100213},
  url = {https://doi.org/10.1016/j.xhgg.2023.100213}
}

RIS

TY  - JOUR
TI  - Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects
AU  - Jessica X. Chong
AU  - Matthew Carter Childers
AU  - Colby T. Marvin
AU  - Allison J. Marcello
AU  - Hernan Gonorazky
AU  - Lili-Naz Hazrati
AU  - James J. Dowling
AU  - Fatema Al Amrani
AU  - Yasemin Alanay
AU  - Yolanda Nieto
AU  - Miguel Á Marín Gabriel
AU  - Arthur S. Aylsworth
AU  - Kati J. Buckingham
AU  - Kathryn M. Shively
AU  - Olivia Sommers
AU  - Kailyn Anderson
AU  - Michael Regnier
AU  - Michael J. Bamshad
PY  - 2023
JO  - Human Genetics and Genomics Advances
DO  - 10.1016/j.xhgg.2023.100213
UR  - https://doi.org/10.1016/j.xhgg.2023.100213
ER  - 

APA

Chong, J. X., Childers, M. C., Marvin, C. T., Marcello, A. J., Gonorazky, H., Hazrati, L., Dowling, J. J., Amrani, F. A., Alanay, Y., Nieto, Y., Gabriel, M. Á. M., Aylsworth, A. S., Buckingham, K. J., Shively, K. M., Sommers, O., Anderson, K., Regnier, M., & Bamshad, M. J. (2023). Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects. Human Genetics and Genomics Advances. https://doi.org/10.1016/j.xhgg.2023.100213

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