The publisher would like to draw the reader's attention to an error in the following article:

Watts GF, Juniper A, van Bockxmeer F, Ademi Z, Liew D, O'Leary P. Familial hypercholesterolaemia: a review with emphasis on evidence for treatment, new models of care and health economic evaluations. Int J Evid Based Healthc 2012; 10: 211-21.

The sentence, on page 213, left column, line 8, should read: The prevalence of compound heterozygous FH (two different mutations) is considered to be one per million (1/500 x 1/500 x 1/4) and true homozygous FH (same mutation) much less than one per million.

The publisher apologises for the above error and any confusion it may have caused.