Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A SLC20A2 mutation identified in an asymptomatic patient with brain calcification.

Journal of the neurological sciences - 15 Jan 2017

Gagliardi Monica, Morelli Maurizio, Iannello Grazia, Colica Carmela, Annesi Grazia, Quattrone Aldo

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain
Share to Brain Diseases
Share to Calcinosis
Share to Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Sodium-Phosphate Cotransporter Proteins, Type III

Source

Identifiers

PMID: 28017251
DOI: 10.1016/j.jns.2016.11.038

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A SLC20A2 mutation identified in an asymptomatic patient with brain calcification.PMID 28017251Read ↗

Novel mutation of SLC20A2 in a Chinese family with primary familial brain calcification.Semantic proximity Read ↗

First report of a de novo mutation at SLC20A2 in a patient with brain calcification.Semantic proximity Read ↗

Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification.Semantic proximity Read ↗

Update and Mutational Analysis of SLC20A2: A Major Cause of Primary Familial Brain Calcification.Semantic proximity Read ↗

Novel SLC20A2 mutation in primary familial brain calcification with disturbance of sustained phonation and orofacial apraxia.Semantic proximity Read ↗

Novel likely pathogenic SLC20A variant in primary familial brain calcification.Semantic proximity Read ↗

Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series.Semantic proximity Read ↗

Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2.Semantic proximity Read ↗

Primary familial brain calcification: Genetic analysis and clinical spectrum.Semantic proximity Read ↗

Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencingSemantic proximity Read ↗

Primary brain calcification: an international study reporting novel variants and associated phenotypes.Semantic proximity Read ↗

Primary familial brain calcifications linked with a novel SLC20A2 gene mutation in a Chinese family.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.