Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification

Neurogenetics. 2014 Aug;15(3):215-6. doi: 10.1007/s10048-014-0404-2. Epub 2014 Apr 27.

Authors

Gaël Nicolas¹, Anne-Claire Richard, Cyril Pottier, Christophe Verny, Franck Durif, Emmanuel Roze, Pascal Favrole, Gabrielle Rudolf, Mathieu Anheim, Christine Tranchant, Thierry Frebourg, Dominique Campion, Didier Hannequin

Affiliation

¹ Department of Genetics, Rouen University Hospital, Rouen, France, gaelnicolas@hotmail.com.

PMID: 24770784
DOI: 10.1007/s10048-014-0404-2

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't
Comment

MeSH terms

Basal Ganglia Diseases / genetics*
Calcinosis / genetics*
Female
Humans
Male
Mutation*
Neurodegenerative Diseases / genetics*
Sodium-Phosphate Cotransporter Proteins, Type III / genetics*

Substances

Sodium-Phosphate Cotransporter Proteins, Type III