Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
Acta Neuropathol Commun
; 9(1): 25, 2021 02 12.
Article
in En
| MEDLINE
| ID: mdl-33579389
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Parkinson Disease
/
Proteins
/
Mutation, Missense
/
Lewy Body Disease
/
Heterozygote
/
Homozygote
Type of study:
Prognostic_studies
Limits:
Aged
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Acta Neuropathol Commun
Year:
2021
Type:
Article
Affiliation country:
Belgium