German, A.; Jukic, J.; Laner, A.; Arnold, P.; Socher, E.; Mennecke, A.; Schmidt, M.A.; Winkler, J.; Abicht, A.; Regensburger, M.
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes 2024, 15, 14.
https://doi.org/10.3390/genes15010014
AMA Style
German A, Jukic J, Laner A, Arnold P, Socher E, Mennecke A, Schmidt MA, Winkler J, Abicht A, Regensburger M.
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes. 2024; 15(1):14.
https://doi.org/10.3390/genes15010014
Chicago/Turabian Style
German, Alexander, Jelena Jukic, Andreas Laner, Philipp Arnold, Eileen Socher, Angelika Mennecke, Manuel A. Schmidt, Jürgen Winkler, Angela Abicht, and Martin Regensburger.
2024. "Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35)" Genes 15, no. 1: 14.
https://doi.org/10.3390/genes15010014
APA Style
German, A., Jukic, J., Laner, A., Arnold, P., Socher, E., Mennecke, A., Schmidt, M. A., Winkler, J., Abicht, A., & Regensburger, M.
(2024). Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes, 15(1), 14.
https://doi.org/10.3390/genes15010014