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

[Clinical features of familial idiopathic basal ganglia calcification caused by a novel mutation in the SLC20A2 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Feb 2015

Zhu Min, Fang Cheng, Li Xiaobing, Zhou Meihong, Wan Hui, Hong Daojun

Abstract excerpt

OBJECTIVE: To describe clinical and genetic feature in a Chinese family with familial idiopathic basal ganglia calcification 3 (IBGC-3) caused by a novel mutation in the SLC20A2 gene. METHODS: Clinical data was collected from a family with familial IBGC-3. All of the family members underwent cere...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Basal Ganglia Diseases
Share to Calcinosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Neurodegenerative Diseases

Share to Sodium-Phosphate Cotransporter Proteins, Type III

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 25636102
DOI: 10.3760/cma.j.issn.1003-9406.2015.01.014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25636102-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Clinical features of familial idiopathic basal ganglia calcification caused by a novel mutation in the SLC20A2 gene].PMID 25636102Read ↗

Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan.Semantic 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 ↗

Association between a novel mutation in SLC20A2 and familial idiopathic basal ganglia calcification.Semantic proximity Read ↗

SLC20A2-related primary familial brain calcification with purely acute psychiatric symptoms: a case report.Semantic proximity Read ↗

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

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

[Molecular mechanism of idiopathic basal ganglia calcification].Semantic proximity Read ↗

Severe brain calcification and migraine headache caused by SLC20A2 and PDGFRB heterozygous mutations in a five-year-old Chinese girl.Semantic proximity Read ↗

Induced pluripotent stem cells derived from a patient with familial idiopathic basal ganglia calcification (IBGC) caused by a mutation in SLC20A2 gene.Semantic proximity Read ↗

Identification of a novel genetic locus on chromosome 8p21.1–q11.23 for idiopathic basal ganglia calcificationSemantic proximity Read ↗

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

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