The Genetics of Parkinson’s Disease and Implications for Clinical Practice
Jacob Day(University of Exeter), Stephen Mullin(University Hospitals Plymouth NHS Trust)
Cited by 221
Related Papers
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia
|Brain|2022|37
Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation
|The American Journal of Human Genetics|2025|5