Two errors were found on p. 70 of the following article appearing on pp. 67–71 of Ophthalmic Genetics, Vol. 29, No. 2:
MUTATION REPORT
Heterozygous FOXC1 Mutation (M161K) Associated with Congenital Glaucoma and Aniridia in an Infant and a Milder Phenotype in Her Mother
Arif O. Khan
Pediatric Ophthalmology Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia
Mohammad A. Aldahmesh
Arabian Diagnostic Laboratories, King Faisal Hospital and Research Center, Riyadh, Saudi Arabia
Abdullah Al-Amri
Emergency Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia
In the caption for Figure 4, the final sentence is incorrect.
“This change is printed as “ANG” for the child because the machine did not decipher the AAG sequence”.
The word childshould be replaced by the word mother, so that the corrected legend should be:
“This change is printed as “ANG” for the mother because the machine did not decipher the AAG sequence”
Also, on p. 70, four lines above the References section:
“We are recently aware of another patient from our institution4 originally diagnosed as congenital glaucoma with clinical aniridia for whom PAX6 sequencing was normal but for whom diagnostic FOXC1 sequencing revealed a W153G mutation.”
W153G is incorrect and should be replaced by W152G, so that the corrected sentence should be:
“We are recently aware of another patient from our institution4 originally diagnosed as congenital glaucoma with clinical aniridia for whom PAX6 sequencing was normal but for whom diagnostic FOXC1 sequencing revealed a W152G mutation.”