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

The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.

Parkinsonism & related disorders - 1 Mar 2015

Saigoh Kazumasa, Mitsui Jun, Hirano Makito, Shioyama Mitsuaki, Samukawa Makoto, Ichikawa Yaeko, Goto Jun, Tsuji Shoji, Kusunoki Susumu

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 Age of Onset
Share to Brain Stem
Share to Cerebellum
Share to Enkephalins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family Health

Share to Protein Precursors

Share to Spinocerebellar Degenerations

Source

Identifiers

PMID: 25595316
DOI: 10.1016/j.parkreldis.2014.12.028

Genes

PDYN

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

The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN gene.PMID 25595316Read ↗

Spinocerebellar Ataxia Type 23 (SCA23): a rare cause of SCA in the AmericasSemantic proximity Read ↗

New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.Semantic proximity Read ↗

Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population.Semantic proximity Read ↗

Novel De Novo KCND3 Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia.Semantic proximity Read ↗

Autosomal recessive spinocerebellar ataxias in Japan.Semantic proximity Read ↗

Motor neuron disease of very long disease duration or Charcot-Marie-Tooth disease? A novel phenotype related to the SOD1 p.E22G variant.Semantic proximity Read ↗

Spinocerebellar ataxia type 23: a genetic update.Semantic proximity Read ↗

The first case of infantile-onset multisystem neurologic, endocrine, and pancreatic disease caused by novel PTRH2 mutation in Japan.Semantic proximity Read ↗

Mutation analysis of PARK2 in a Uyghur family with early-onset Parkinson's disease in Xinjiang, China.Semantic proximity Read ↗

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

Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease.Semantic proximity Read ↗

HNPP due to a novel missense mutation of the PMP22 gene.Semantic proximity Read ↗

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