Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy - Archive ouverte HAL Access content directly
Journal Articles Human Mutation Year : 2019

Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy

Alexandre Janin
Valérie Chanavat
  • Function : Author
Karine Nguyen
Philippe Chevalier
  • Function : Author
Jean‐christophe Eicher
  • Function : Author
Laurence Faivre
  • Function : Author
Juliette Piard
  • Function : Author
Emma Albert
  • Function : Author
Severine Nony
  • Function : Author
Gilles Millat
  • Function : Author

Dates and versions

hal-04383056 , version 1 (09-01-2024)

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Alexandre Janin, Valérie Chanavat, Pierre‐antoine Rollat-Farnier, Claire Bardel, Karine Nguyen, et al.. Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy. Human Mutation, 2019, 41 (2), pp.465-475. ⟨10.1002/humu.23944⟩. ⟨hal-04383056⟩
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