Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family

  1. Perez de Nanclares, G.
  2. Castaño, L.
  3. Martul, P.
  4. Rica, I.
  5. Vela, A.
  6. Sanjurjo, P.
  7. Aldamiz-Echevarría, K.
  8. Martinez, R.
  9. Sarrionandia, M.J.
Aldizkaria:
Journal of Pediatric Endocrinology and Metabolism

ISSN: 0334-018X

Argitalpen urtea: 2001

Alea: 14

Zenbakia: 3

Orrialdeak: 295-300

Mota: Artikulua

DOI: 10.1515/JPEM.2001.14.3.295 GOOGLE SCHOLAR