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

Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy.

Journal of Zhejiang University. Science. B - 1 Jan 2009

Liang Yu-hua, Chen Xiao-ling, Yu Zhong-sheng, Chen Chun-yue, Bi Sheng, Mao Lian-gen, Zhou Bo-lin, Zhang Xian-ning

Abstract excerpt

Spinal muscular atrophy (SMA) is a disorder characterized by degeneration of lower motor neurons and occasionally bulbar motor neurons leading to progressive limb and trunk paralysis as well as muscular atrophy. Three types of SMA are recognized depending on the age of onset, the maximum muscular activity achieved, and survivorship: SMA1, SMA2, and SMA3. The survival of motor neuron (SMN) gene has been identified...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Deletion

Share to Incidence

Share to Infant

Share to Spinal Muscular Atrophies of Childhood

Share to Survival of Motor Neuron 1 Protein

Source

Open in PubMed Open full text

Identifiers

PMID: 19198020
DOI: 10.1631/jzus.B0820125
PMCID: PMC2613960

Genes

NAIP
SMN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Deletion analysis of SMN1 and NAIP genes in Southern Chinese children with spinal muscular atrophy.PMID 19198020Read ↗

NAIP Gene Deletion and SMN2 Copy Number as Molecular Tools in Predicting the Severity of Spinal Muscular Atrophy.Semantic proximity Read ↗

The analysis of the association between the copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein genes and the clinical phenotypes in 40 patients with spinal muscular atrophy: Observational study.Semantic proximity Read ↗

Mutation Spectrum of the Survival of Motor Neuron 1 and Functional Analysis of Variants in Chinese Spinal Muscular Atrophy.Semantic proximity Read ↗

Deletions in the survival motor neuron gene in Iranian patients with spinal muscular atrophy.Semantic proximity Read ↗

Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controlsSemantic proximity Read ↗

Molecular analysis of SMN, NAIP and P44 genes of SMA patients and their families.Semantic proximity Read ↗

Mutation analysis of 419 family and prenatal diagnosis of 339 cases of spinal muscular atrophy in China.Semantic proximity Read ↗

Establishment of a molecular diagnostic system for spinal muscular atrophy experience from a clinical laboratory in china.Semantic proximity Read ↗

Gene deletion patterns in spinal muscular atrophy patients with different clinical phenotypes.Semantic proximity Read ↗

Deletion analysis of spinal muscular atrophy in southern Indian population.Semantic proximity Read ↗

Application of DNA-based tests for diagnosis of spinal muscular atrophy in Saudi Arabia.Semantic proximity Read ↗

Carrier Screening of SMA in North ChinaSemantic proximity Read ↗

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