A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia

  1. Rivera, B.
  2. Perea, J.
  3. Sánchez, E.
  4. Villapún, M.
  5. Sánchez-Tomé, E.
  6. Mercadillo, F.
  7. Robledo, M.
  8. Benítez, J.
  9. Urioste, M.
Revue:
European Journal of Human Genetics

ISSN: 1018-4813 1476-5438

Année de publication: 2014

Volumen: 22

Número: 3

Pages: 423-426

Type: Article

DOI: 10.1038/EJHG.2013.146 GOOGLE SCHOLAR lock_openAccès ouvert editor

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