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PDFPhenotypes
Short report
Expanding the phenotype of COPA syndrome: a kindred with typical and atypical features
- Correspondence to Dr Bernadette R Gochuico, Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892-1851, USA; gochuicb{at}mail.nih.gov
Citation
Expanding the phenotype of COPA syndrome: a kindred with typical and atypical features
Publication history
- Received July 20, 2018
- Revised September 14, 2018
- Accepted September 30, 2018
- First published November 1, 2018.
Online issue publication
October 23, 2019
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© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.