| Literature DB >> 10854116 |
J D Hamlington1, M V Clough, J A Dunston, I McIntosh.
Abstract
Nail patella syndrome (NPS) has been shown to result from loss of function mutations within the transcription factor LMX1B. In a large NPS family a 17 bp intronic deletion encompassing a consensus branchpoint sequence was observed to segregate with the NPS phenotype. RNA analysis demonstrated that deletion of the branchpoint sequence resulted in skipping of the downstream exon. A mechanism to explain this phenomenon is presented.Entities:
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Year: 2000 PMID: 10854116 DOI: 10.1038/sj.ejhg.5200448
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246