A single-residue mutation, G203E, causes 3-hydroxy-3-methylglutaric aciduria by occluding the substrate channel in the 3D structural model of HMG-CoA lyase

Citation
Mir, C., Lopez‐Viñas, E., Aledo, R., Puisac, B., Rizzo, C., Dionisi‐Vici, C., Deodato, F., Pié, J., Gomez‐Puertas, P., Hegardt, F. G., & Casals, N. (2006). A single‐residue mutation, G203E, causes 3‐hydroxy‐3‐methylglutaric aciduria by occluding the substrate channel in the 3D structural model of HMG‐CoA lyase. Journal of Inherited Metabolic Disease, 29(1), 64–70. Portico. https://doi.org/10.1007/s10545-006-0138-x
DOI:
DOI: 10.1007/s10545-006-0138-x
Year of publication:
2006