Article title: Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations
Authors: Nutsuchar Wangtiraumnuay, Waleed Abed Alnabi, Mai Tsukikawa, Avrey Thau, Jenina Capasso,
Reuven Sharony, Chris F. Inglehearrn, and Alex V. Levin
Journal: Ophthalmic Genetics
Bibliometrics: 2018, Vol. 39, No. 3, pp. 384–390
DOI: 10.1080/13816810.2018.1432063
When the above article was published online and in print, in the Discussion section, the reference citation of the following sentence was written incorrectly: “SNHL can be unilateral or bilateral and nails can be normal (7–9).”
The corrected reference citation should be as follows: “SNHL can be unilateral or bilateral and nails can be normal (7–8).”
Moreover, in the reference list, reference 9 should be:
Parry DA, Mighell AJ, El-Sayed W, Shore RC, Jalili IK, Dollfus H, Bloch-Zupan A, Carlos R, Carr IM, Downey LM, et al. Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. Am J Hum Genet 2009;84(2):266-73.
The authors apologize for this error.