Naturally-occurring rare mutations cause mild to catastrophic effects in the multifunctional and cancer-associated NQO1 protein

  1. Pacheco-García, J.L.
  2. Cano-Muñoz, M.
  3. Sánchez-Ramos, I.
  4. Salido, E.
  5. Pey, A.L.
Revue:
Journal of Personalized Medicine

ISSN: 2075-4426

Année de publication: 2020

Volumen: 10

Número: 4

Pages: 1-31

Type: Article

DOI: 10.3390/JPM10040207 GOOGLE SCHOLAR lock_openAccès ouvert editor
La source de données: Scopus