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Article

A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variation.

Neurogenetics - 1 May 1997

Novelli G, Semprini S, Capon F, Dallapiccola B

Abstract excerpt

Childhood SMAs are common neuromuscular disorders, due to the occurrence of large genomic deletions encompassing the SMN gene and often extending to involve the NAIP gene. Although NAIP deletions are more frequently observed in patients affected by the acute form of the disease, it is not possibl...

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Share to Cyclic AMP Response Element-Binding Protein
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscular Atrophy, Spinal

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Source

Identifiers

PMID: 10735271
DOI: 10.1007/s100480050004

Genes

NAIP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10735271-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variation.PMID 10735271Read ↗

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Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.Semantic proximity Read ↗

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

Genetic pattern of SMN1, SMN2, and NAIP genes in prognosis of SMA patientsSemantic proximity Read ↗

SMN(T) and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): genotype/phenotype correlations with disease severity.Semantic proximity Read ↗

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