Multiplex analysis of the most common mutations related to hereditary haemochromatosis: Two methods combining specific amplification with capillary electrophoresis

  1. Gômez-Llorente, C.
  2. Antúnez, A.
  3. Blanco, S.
  4. Suarez, A.
  5. Gömez-Capilla, J.A.
  6. Farez-Vidal, M.E.
Aldizkaria:
European Journal of Haematology

ISSN: 0902-4441

Argitalpen urtea: 2004

Alea: 72

Zenbakia: 2

Orrialdeak: 121-129

Mota: Artikulua

DOI: 10.1046/J.0902-4441.2003.00186.X GOOGLE SCHOLAR