| Literature DB >> 12658451 |
Stephan Niemann1, Ulrich Müller, Dieter Engelhardt, Peter Lohse.
Abstract
Mutations in SDHC cause autosomal dominant paraganglioma, type 3 (PGL3), and have to date been demonstrated in only one family. Here, we report on a novel mutation in a patient with a malignant, catecholamine-producing paraganglioma at the carotid bifurcation. The mutation is a G-->T transversion at position +1 of intron 5 of the SDHC gene, leading to the deletion of exon 5 and a shift in the reading frame.Entities:
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Year: 2003 PMID: 12658451 DOI: 10.1007/s00439-003-0938-0
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132