*Inserm UMR1231 Team GAD, University of Burgundy and Franche-Comté
†Genetics Center, FHU-TRANSLAD
‡Neurology Department
§Functional Unity of Innovative Diagnosis for Rare Diseases, Dijon Bourgogne University Hospital, Dijon, France
G.D. and C.T.-R.: conceptualization. Q.T., G.D., S.N., and C.P.: data curation. Q.T. and Y.D.: methodology. Q.T., G.D., C.T.-R., Y.B. and L.F.: supervision. Q.T. and G.D.: visualization. Q.T., G.D., and C.T.-R.: writing—original draft.
Patient gave her written consent for the anonymous publication of her clinical, imaging and sequencing data.
The authors declare no conflicts of interest.
Reprints: Quentin Thomas, MD, FHU-TRANSLAD, Centre de Génétique, Hôpital d’Enfants, CHU Dijon Bourgogne, Dijon 21000, France (e-mail: [email protected]).
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