Li, T., Kou, D., Cui, Y., & Le, W. (2020). Whole exome sequencing identified a new compound heterozygous PRKN mutation in a Chinese family with early-onset Parkinson’s disease. Biosci Rep.
Styl ChicagoLi, Tianbai, Daqing Kou, Yanhua Cui, a Weidong Le. "Whole Exome Sequencing Identified a New Compound Heterozygous PRKN Mutation in a Chinese Family With Early-onset Parkinson’s Disease." Biosci Rep 2020.
Citace podle MLALi, Tianbai, Daqing Kou, Yanhua Cui, a Weidong Le. "Whole Exome Sequencing Identified a New Compound Heterozygous PRKN Mutation in a Chinese Family With Early-onset Parkinson’s Disease." Biosci Rep 2020.
Upozornění: Tyto citace jsou generovány automaticky. Nemusí být zcela správně podle citačních pravidel..