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. 2018 Nov 1;103(5):826. doi: 10.1016/j.ajhg.2018.10.002

Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

Shereen G Ghosh, Kerstin Becker, He Huang, Tracy Dixon-Salazar, Guoliang Chai, Vincenzo Salpietro, Lihadh Al-Gazali, Quinten Waisfisz, Haicui Wang, Keith K Vaux, Valentina Stanley, Andreea Manole, Ugur Akpulat, Marjan M Weiss, Stephanie Efthymiou, Michael G Hanna, Carlo Minetti, Pasquale Striano, Livia Pisciotta, Elisa De Grandis, Janine Altmüller, Peter Nürnberg, Holger Thiele, Uluc Yis, Tuncay Derya Okur, Ayse Ipek Polat, Nafise Amiri, Mohammad Doosti, Ehsan Ghayoor Karimani, Mehran B Toosi, Gabriel Haddad, Mert Karakaya, Brunhilde Wirth, Johanna M van Hagen, Nicole I Wolf, Reza Maroofian, Henry Houlden, Sebahattin Cirak ∗, Joseph G Gleeson ∗∗
PMCID: PMC6218605  PMID: 30388405

(The American Journal of Human Genetics 103, 431–439; September 6, 2018)

In the original version of this article, author Tracy Dixon-Salazar’s name was incomplete. It now appears correctly here and online. The authors regret the error.

Contributor Information

Sebahattin Cirak, Email: sebahattin.cirak@uk-koeln.de.

Joseph G. Gleeson, Email: jogleeson@ucsd.edu.

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

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