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.
Revista:
European Journal of Haematology

ISSN: 0902-4441

Any de publicació: 2004

Volum: 72

Número: 2

Pàgines: 121-129

Tipus: Article

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