A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency

  1. Quinzii, C.
  2. Naini, A.
  3. Salviati, L.
  4. Trevisson, E.
  5. Navas, P.
  6. DiMauro, S.
  7. Hirano, M.
Revue:
American Journal of Human Genetics

ISSN: 0002-9297

Année de publication: 2006

Volumen: 78

Número: 2

Pages: 345-349

Type: Article

DOI: 10.1086/500092 GOOGLE SCHOLAR lock_openAccès ouvert editor
La source de données: Scopus