Development of a high-resolution melting method for mutation detection in familial hypercholesterolaemia patients.

Míreanna comhchosúla

• Statins and familial hypercholesterolaemia.
  de réir: Neil, A, et al.
  Foilsithe / Cruthaithe: (2009)
• DEVELOPMENT OF AN AFFORDABLE, SENSITIVE AND RAPID SCREENING METHOD FOR MUTATION DETECTION IN UK FH SUBJECTS
  de réir: Scartezini, M, et al.
  Foilsithe / Cruthaithe: (2008)
• Controversies in familial hypercholesterolaemia: recommendations of the NICE Guideline Development Group for the identification and management of familial hypercholesterolaemia.
  de réir: Minhas, R, et al.
  Foilsithe / Cruthaithe: (2009)
• The utility of DNA-based testing in patients with familial hypercholesterolaemia in the UK
  de réir: Humphries, SE, et al.
  Foilsithe / Cruthaithe: (2005)
• Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations.
  de réir: Futema, M, et al.
  Foilsithe / Cruthaithe: (2014)