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Loss or Gain of Function Mutations in ACOX1 Cause Axonal Loss Via Different Mechanisms

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Year: 2019
Type: preprint
Source: SSRN Electronic Journal
DOI: 10.2139/ssrn.3443598
Authors: Hyunglok Chung, Michael F. Wangler, Paul Marcogliese, Juyeon Jo, Thomas Ravenscoft, Lita Duraine, Sina Sadeghzadeh, David Li-Kroeger, Robert E. Schmidt, Alan Pestronk, Jill Rosenfeld, Lindsay Burrage, Mitchell Herndon, Shan Chen, Undiagnosed Diseases Network Group, Amelle Shillington, Marissa Vawater-Lee, Robert Hopkin, Jackeline Rodriguez-Smith, Michael Henrickson, Brendan Lee, Ann Moser, Richard O. Jones, Taekyeong Yoo, Soe Mar, Murim Choi, Robert Bucelli, Shinya Yamamoto, Hyun Kyung Lee, Carlos Prada, Jong-Hee Chae, Tiphanie Vogel, Hugo Bellen
Institutions: Howard Hughes Medical Institute, Baylor University, Baylor College of Medicine, Harvard University, Washington University in St. Louis, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Johns Hopkins University, Seoul National University, Seoul National University Children's Hospital, University of Chicago
Language: English

Topic: Hereditary Neurological Disorders
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green
OpenAlex ID: W3123957724
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Related to: 10
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