Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
Neurogenetics
; 14(1): 11-22, 2013 Feb.
Article
in En
| MEDLINE
| ID: mdl-23334463
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Basal Ganglia Diseases
/
Calcinosis
/
Neurodegenerative Diseases
/
Sodium-Phosphate Cotransporter Proteins, Type III
/
Mutation
Type of study:
Etiology_studies
/
Incidence_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adult
/
Aged
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Neurogenetics
Journal subject:
GENETICA
/
NEUROLOGIA
Year:
2013
Type:
Article
Affiliation country:
United States