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

Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification.

European journal of neurology - 1 Mar 2013

Lemos R R, Oliveira M F, Oliveira J R M

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 Aged, 80 and over
Share to Basal Ganglia Diseases
Share to Brazil
Share to Calcinosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Neurodegenerative Diseases

Share to Pedigree

Share to Sodium-Phosphate Cotransporter Proteins, Type III

Source

Identifiers

PMID: 23406454
DOI: 10.1111/ene.12044

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification.PMID 23406454Read ↗

A SLC20A2 mutation identified in an asymptomatic patient with brain calcification.Semantic proximity Read ↗

Novel mutation of SLC20A2 in a Chinese family with 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 ↗

Vertical Supranuclear Gaze Palsy in Primary Familial Brain Calcification Associated with a Novel SLC20A2 MutationSemantic proximity Read ↗

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

A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification.Semantic proximity Read ↗

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.Semantic proximity Read ↗

Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisSemantic proximity Read ↗

A Novel SLC20A2 Mutation Associated with Familial Idiopathic Basal Ganglia Calcification and Analysis of the Genotype-Phenotype Association in Chinese Patients.Semantic proximity Read ↗

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.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 ↗

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