Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy

  1. Estañ, M.C.
  2. Fernández-Núñez, E.
  3. Zaki, M.S.
  4. Esteban, M.I.
  5. Donkervoort, S.
  6. Hawkins, C.
  7. Caparros-Martin, J.A.
  8. Saade, D.
  9. Hu, Y.
  10. Bolduc, V.
  11. Chao, K.R.-Y.
  12. Nevado, J.
  13. Lamuedra, A.
  14. Largo, R.
  15. Herrero-Beaumont, G.
  16. Regadera, J.
  17. Hernandez-Chico, C.
  18. Tizzano, E.F.
  19. Martinez-Glez, V.
  20. Carvajal, J.J.
  21. Zong, R.
  22. Nelson, D.L.
  23. Otaify, G.A.
  24. Temtamy, S.
  25. Aglan, M.
  26. Issa, M.
  27. Bönnemann, C.G.
  28. Lapunzina, P.
  29. Yoon, G.
  30. Ruiz-Perez, V.L.
  31. Show all authors +
Journal:
Nature Communications

ISSN: 2041-1723

Year of publication: 2019

Volume: 10

Issue: 1

Type: Article

DOI: 10.1038/S41467-019-08548-9 GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus