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

Hyung-Lok Chung, Michael F. Wangler, Paul C. Marcogliese, Ju-Yeon Jo, Thomas A. Ravenscroft, Zhongyuan Zuo, Lita Duraine, Sina Sadeghzadeh, David Li‐Kroeger, Robert E. Schmidt, Alan Pestronk, Jill A. Rosenfeld, Lindsay C. Burrage, Mitchell J. Herndon, Shan Chen, Amelle Shillington, Marissa Vawter‐Lee, Robert J. Hopkin, Jackeline Rodriguez‐Smith, Michael Henrickson, Brendan Lee, Ann B. Moser, Richard O. Jones, Paul A. Watkins, Taekyeong Yoo, Soe Mar, Murim Choi, Robert C. Bucelli, Shinya Yamamoto, Hyun Kyoung Lee, Carlos E. Prada, Jong‐Hee Chae, Tiphanie P. Vogel, Hugo J. Bellen

2020Neuron163 citationsDOIOpen Access PDF

Topics & Concepts

PeroxisomeLimitingOxidase testFunction (biology)EnzymeLoss functionChemistryCell biologyBiochemistryBiologyGenePhenotypeEngineeringMechanical engineeringPeroxisome Proliferator-Activated ReceptorsMetabolism and Genetic DisordersMitochondrial Function and Pathology
Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms | Litcius