Litcius/Paper detail

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

Zheng Yie Yap, Stéphanie Efthymiou, Simone Seiffert, Karen Vargas Parra, Sukyeong Lee, Alessia Nasca, Reza Maroofian, Isabelle Schrauwen, Manuela Pendziwiat, Sunhee Jung, Elizabeth Bhoj, Pasquale Striano, Kshitij Mankad, Barbara Vona, Sanmati Cuddapah, Anja Wagner, Javeria Raza Alvi, Elham Davoudi-Dehaghani, Mohammad‐Sadegh Fallah, Srinitya Gannavarapu, Costanza Lamperti, Andrea Legati, Bibi Nazia Murtaza, Muhammad Shahid Nadeem, Mujaddad Ur Rehman, Kolsoum Saeidi, Vincenzo Salpietro, Sarah von Spiczak, Abigail Sandoval, Sirous Zeinali, Massimo Zeviani, Adi Reich, Cholsoon Jang, Ingo Helbig, Tahsin Stefan Barakat, Daniele Ghezzi, Suzanne M. Leal, Yvonne Weber, Henry Houlden, Wan Hee Yoon

2021The American Journal of Human Genetics32 citationsDOIOpen Access PDF

Topics & Concepts

BiologyFrameshift mutationMicrocephalyGeneticsHearing lossAtaxiaMissense mutationAlleleExonPhenotypeGeneMedicineNeuroscienceAudiologyMitochondrial Function and PathologyMetabolism and Genetic DisordersBiochemical and Molecular Research