Molecular analysis of hemophilia A mutations in the Finnish population.

Lignende værker

• A novel missense mutation in the factor VIII gene identified by analysis of amplified hemophilia DNA sequences.
  af: Levinson, B, et al.
  Udgivet: (1987)
• Hemophilia B: molecular pathogenesis and mutation analysis
  af: Goodeve, A. C.
  Udgivet: (2015)
• Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.
  af: Ala-Mello, S, et al.
  Udgivet: (1998)
• Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland.
  af: Guldberg, P, et al.
  Udgivet: (1995)
• A novel mutation in the sulfate transporter gene SLC26A2 (DTDST) specific to the Finnish population causes de la Chapelle dysplasia
  af: Bonafé, L, et al.
  Udgivet: (2008)