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

[Spinocerebellar ataxia-27: description of the clinical phenotype of two twin sisters with a deletion in the FGF14 gene].

Revista de neurologia - 1 Mar 2016

Blanco-Barca Óscar, Amado-Puentes Alfonso, Repáraz Alfredo, Melcón Cristina, Torreira Cristina

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 Child, Preschool
Share to Diseases in Twins
Share to Fibroblast Growth Factors
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sequence Deletion

Share to Spinocerebellar Degenerations

Source

Identifiers

PMID: 26916329

Genes

FGF14

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Spinocerebellar ataxia-27: description of the clinical phenotype of two twin sisters with a deletion in the FGF14 gene].PMID 26916329Read ↗

Spinocerebellar Ataxia 27: Clinical Phenotype of Twin Sisters with FGF14 Deletion.Semantic proximity Read ↗

SCA27 caused by a chromosome translocation: further delineation of the phenotype.Semantic proximity Read ↗

Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.Semantic proximity Read ↗

[Molecular and clinical features of SCA 7].Semantic proximity Read ↗

A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected].Semantic proximity Read ↗

[Genetic basis of sponadic Parkinson disease: common disease-multiple rare variants].Semantic proximity Read ↗

[Report of a family with spinocerebellar ataxia and SCA1 gene mutation].Semantic proximity Read ↗

Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.Semantic proximity Read ↗

Spinocerebellar ataxias type 27 derived from a disruption of the fibroblast growth factor 14 gene with mimicking phenotype of paroxysmal non-kinesigenic dyskinesia.Semantic proximity Read ↗

[Spinocerebellar ataxia 17: full phenotype in a 42 CAG/CAA-repeats carrier].Semantic proximity Read ↗

Spinocerebellar Ataxia 27 A with Episodic Ataxia: Case Series of Fibroblast Growth Factor 14 (FGF14) Microdeletions.Semantic proximity Read ↗

Clinical utility gene card for: Williams-Beuren Syndrome [7q11.23].Semantic proximity Read ↗

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