Genotype–phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France

Author:

Mariani Louise‐Laure1,Lozeron Pierre123,Théaudin Marie124,Mincheva Zoia12,Signate Aissatou5,Ducot Beatrice678,Algalarrondo Vincent2910,Denier Christian149,Adam Clovis211,Nicolas Guillaume1213,Samuel Didier1415,Slama Michel S.2910,Lacroix Catherine211,Misrahi Micheline2916,Adams David124917,

Affiliation:

1. Department of NeurologyBicêtre Hospital Le Kremlin‐Bicêtre;

2. French National Reference Center for Familial Amyloid Polyneuropathies (NNERf) Le Kremlin‐Bicêtre

3. Department of Neurophysiology, APHP, Lariboisière HospitalUniversity Paris-Diderot Sorbonne Paris Cité INSERM UMR-965, Paris, France

4. National Institute of Health and Medical Research Unit U1191 Le Kremlin‐Bicêtre

5. Department of NeurologyPierre Zobda‐Quitman Hospital Fort de France

6. Reproduction and Child Development TeamCenter for Research in Epidemiology and Population Health Le Kremlin‐Bicêtre

7. University of Paris–South Villejuif

8. National Institute for Demographic Studies Paris

9. University Paris–Sud Paris

10. Department of CardiologyAntoine Béclère Hospital Clamart

11. Department of NeuropathologyBicêtre Hospital Le Kremlin‐Bicêtre

12. Department of NeurologyRaymond Poincaré Hospital Garches

13. University of Versailles Saint‐Quentin‐en‐Yvelines Versailles

14. Hepatobiliary Center, Paul Brousse Hospital Villejuif

15. National Institute of Health and Medical Research Mixed Unit of Research S785 Villejuif

16. Department of Molecular BiologyBicêtre Hospital Le Kremlin‐Bicêtre

17. FILNEMUS, Filière nationale de Santé Maladies Rares NeuromusculairesMarseille France

Funder

French Amyloidosis Association

Publisher

Wiley

Subject

Clinical Neurology,Neurology

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