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Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency

Authors
  1. A. A. Garcia
  2. AC Dykes
  3. AM Johansson
  4. B Dahlbäck
  5. B Dahlbäck
  6. B Hurtado
  7. C. A. Spek
  8. CJ Wolf de
  9. CT Esmon
  10. D Borgel
  11. D. Borgel
  12. DA Lane
  13. DK Schmidel
  14. DK Schmidel
  15. E Gómez
  16. E Lanke
  17. H Tatewaki
  18. HK Ploos van Amstel
  19. HK Ploos van Amstel
  20. HS Choung
  21. J Duchemin
  22. J Hoebeeck
  23. JH Yoo
  24. JK Ploos van Amstel
  25. JP Schouten
  26. JT Dunnen den
  27. KE Persson
  28. LFA Maurissen
  29. M. Alhenc-Gelas
  30. M. C. H. de Visser
  31. Maria C. Pintao
  32. MK Kate ten
  33. P García de Frutos
  34. PC Comp
  35. PD Stenson
  36. PH Reitsma
  37. Pieter H. Reitsma
  38. RE Simmonds
  39. S Gandrille
  40. S Gandrille
  41. S. Gandrille
  42. T Yin
  43. U Seligsohn
  44. Y Espinosa-Parrilla
  45. YP Visser de
Publication date
Publisher
'Springer Science and Business Media LLC'
Doi

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      Last time updated on 05/06/2019

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