Fan, Z., Greenwood, R., Felix, A. C. G., Shiloh-Malawsky, Y., Tennison, M., Roche, M., . . . Evans, J. (2014). GCH1 heterozygous mutation identified by whole-exome-sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia.
Citação norma ChicagoFan, Zheng, et al. GCH1 Heterozygous Mutation Identified By Whole-exome-sequencing As a Treatable Condition in a Patient Presenting With Progressive Spastic Paraplegia. 2014.
Citação norma MLAFan, Zheng, et al. GCH1 Heterozygous Mutation Identified By Whole-exome-sequencing As a Treatable Condition in a Patient Presenting With Progressive Spastic Paraplegia. 2014.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.