Functional Validation of a COPA Mutation Broadens the Spectrum of COPA Syndrome

The authors would like to thank Dr. Alix de Becdelièvre for the genetic analysis performed by her team at the Molecular Genetics Department, Mondor Hospital, AP-HP, Paris, France. The authors would also like to acknowledge Gillian I Rice and Luis Seabra for the assessment of interferon scores, and Prof. Yanick Crow for insightful discussions. C.D. is supported by the Fondation pour la Recherche Médicale (Grant: FDM202106013329). M-L.F. acknowledges the Square Foundation.

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