Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2

Neurol Sci. 2018 Feb;39(2):379-380. doi: 10.1007/s10072-017-3125-0. Epub 2017 Sep 21.

Authors

Carmelina Chiriaco¹, Fabiana Novellino², Maria Salsone², Monica Gagliardi², Maurizio Morelli³, Aldo Quattrone^{2

3}

Affiliations

¹ Institute of Molecular Bioimaging and Physiology, National Research Council, (IBFM-CNR) Section of Germaneto, Catanzaro, Italy. cchiriaco@gmail.com.
² Institute of Molecular Bioimaging and Physiology, National Research Council, (IBFM-CNR) Section of Germaneto, Catanzaro, Italy.
³ Department of Medical and Surgical Science, Institute Of Neurology, University Magna Graecia, Catanzaro, Germaneto, Italy.

PMID: 28936702
DOI: 10.1007/s10072-017-3125-0

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Brain Diseases / complications
Brain Diseases / genetics*
Calcinosis / complications
Calcinosis / genetics*
Cognition Disorders / etiology
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Mutation / genetics*
Psychiatric Status Rating Scales
Sodium-Phosphate Cotransporter Proteins, Type III / genetics*

Substances

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