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

Topics Community

Article

Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.

Chinese medical journal - 5 Sept 2009

Du Juan, Shen Lu, Zhao Guo-hua, Wang Yin-guang, Liao Shu-sheng, Chen Chong, Zhou Zhi-fan, Luo Ying-ying, Jiang Hong, Xia Kun, Tang Bei-sha

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 Asian People
Share to Child, Preschool
Share to Infant
Share to Membrane Transport Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymerase Chain Reaction

Share to Sequence Analysis, DNA

Share to Spastic Paraplegia, Hereditary

Share to Young Adult

Source

Identifiers

PMID: 19781397

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.PMID 19781397Read ↗

A clinical and genetic study of SPG31 in Japan.Semantic proximity Read ↗

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.Semantic proximity Read ↗

Spastic paraplegia type 31: A novel REEP1 splice site donor variant and expansion of the phenotype variability.Semantic proximity Read ↗

Erratum: Mutation Analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic ParaplegiaSemantic proximity Read ↗

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.Semantic proximity Read ↗

A novel homozygous mutation in ERLIN1 gene causing spastic paraplegia 62 and literature review.Semantic proximity Read ↗

Genotype-phenotype study and expansion of ARL6IP1-related complicated hereditary spastic paraplegia.Semantic proximity Read ↗

Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic ParaplegiaSemantic proximity Read ↗

Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31).Semantic proximity Read ↗

New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP).Semantic proximity Read ↗

Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4)Semantic proximity Read ↗

Clinical and genetic study of a novel mutation in the REEP1 gene.Semantic proximity Read ↗

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