(The American Journal of Human Genetics 86, 248–253; February 12, 2010)
On page 249 of the originally published paper, the following text appears: “We first identified a 7 bp insertion in exon 4, c.218_219insGCTCTTT, in an Australian family of European descent (family 1).” The mutation includes a typo and should instead read “c.218_219insGCTGTTT.” The term appears correctly in Figure 2.
On the same page, the following text also includes a typo: “The fourth mutation identified was a 5 bp deletion at the end of intron 5, c.361-1_361-5delACCAG, in an isolated FEVR patient from the UK.” The mutation should instead read “c.361-5_361-1delACCAG” and appears correctly in Figure 2.
The authors apologize for these errors.