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Article

Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing.

American journal of human genetics - 1 Feb 2006

Hiller Michael, Huse Klaus, Szafranski Karol, Jahn Niels, Hampe Jochen, Schreiber Stefan, Backofen Rolf, Platzer Matthias

Abstract excerpt

Aberrant or modified splicing patterns of genes are causative for many human diseases. Therefore, the identification of genetic variations that cause changes in the splicing pattern of a gene is important. Elsewhere, we described the widespread occurrence of alternative splicing at NAGNAG acceptors. Here, we report a genomewide screen for single-nucleotide polymorphisms (SNPs) that affect such tandem acceptors....

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Identifiers

PMID: 16400609
DOI: 10.1086/500151
PMCID: PMC1380236

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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.

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