Novel mutation of SLC20A2 in an Italian patient presenting with migraine

J Neurol. 2014 Oct;261(10):2019-21. doi: 10.1007/s00415-014-7475-8. Epub 2014 Sep 2.

Authors

Elisa Rubino¹, Elisa Giorgio, Salvatore Gallone, Lorenzo Pinessi, Laura Orsi, Salvatore Gentile, Sergio Duca, Alfredo Brusco

Affiliation

¹ Neurology I, Department of Neuroscience "Rita Levi Montalcini", University of Torino, Via Cherasco 15, 10126, Torino, Italy, [email protected].

PMID: 25178512
DOI: 10.1007/s00415-014-7475-8

No abstract available

Publication types

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

MeSH terms

Brain / pathology
DNA Mutational Analysis
Female
Humans
Italy
Middle Aged
Migraine Disorders / genetics*
Migraine Disorders / pathology
Mutation / genetics*
Sodium-Phosphate Cotransporter Proteins, Type III / genetics*
Tomography, X-Ray Computed

Substances

SLC20A2 protein, human
Sodium-Phosphate Cotransporter Proteins, Type III