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. 2018 Apr 5;102(4):713. doi: 10.1016/j.ajhg.2018.03.020

Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa

Andrea Angius, Paolo Uva, Insa Buers, Manuela Oppo, Alessandro Puddu, Stefano Onano, Ivana Persico, Angela Loi, Loredana Marcia, Wolfgang Höhne, Gianmauro Cuccuru, Giorgio Fotia, Manila Deiana, Mara Marongiu, Hatice Tuba Atalay, Sibel Inan, Osama El Assy, Leo ME Smit, Ilyas Okur, Koray Boduroglu, Gülen Eda Utine, Esra Kılıç, Giuseppe Zampino, Giangiorgio Crisponi, Laura Crisponi ∗, Frank Rutsch
PMCID: PMC5985354  PMID: 29625027

(The American Journal of Human Genetics 99; 236–245, July 7, 2016)

In Table 1 of this article, the “cold-induced sweating” row incorrectly contains a plus sign for individual CS_258 instead of a minus sign. That is, the authors did not observe cold-induced sweating for any individuals in the cohort with mutations in KLHL7. The authors apologize for the error and any confusion it may have caused.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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