Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy

  1. Ochoa, J.P.
  2. Lopes, L.R.
  3. Perez-Barbeito, M.
  4. Cazón-Varela, L.
  5. de la Torre-Carpente, M.M.
  6. Sonicheva-Paterson, N.
  7. De Uña-Iglesias, D.
  8. Quinn, E.
  9. Kuzmina-Krutetskaya, S.
  10. Garrote, J.A.
  11. Elliott, P.M.
  12. Monserrat, L.
Journal:
Clinical Genetics

ISSN: 1399-0004 0009-9163

Year of publication: 2020

Volume: 98

Issue: 1

Pages: 86-90

Type: Article

DOI: 10.1111/CGE.13759 GOOGLE SCHOLAR