A Recurrent Stop-Codon Mutation in Succinate Dehydrogenase Subunit B Gene in Normal Peripheral Blood and Childhood T-Cell Acute Leukemia
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference23 articles.
1. Signaling pathways in acute oxygen sensing; Novartis Foundation symposium,2006
2. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.;BE Baysal;Science,2000
3. The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.;JP Bayley;BMC Med Genet,2005
4. A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas.;PL Dahia;PLoS Genet,2005
5. Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect.;K Astrom;Hum Genet,2003
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