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Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification.
- Source :
-
European journal of neurology [Eur J Neurol] 2013 Mar; Vol. 20 (3), pp. e43-e44. - Publication Year :
- 2013
- Subjects :
- Adult
Aged, 80 and over
Basal Ganglia Diseases physiopathology
Brazil
Calcinosis physiopathology
Female
Humans
Male
Mutation
Neurodegenerative Diseases physiopathology
Pedigree
Basal Ganglia Diseases genetics
Calcinosis genetics
Neurodegenerative Diseases genetics
Sodium-Phosphate Cotransporter Proteins, Type III genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1468-1331
- Volume :
- 20
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- European journal of neurology
- Publication Type :
- Report
- Accession number :
- 23406454
- Full Text :
- https://doi.org/10.1111/ene.12044