The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway
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| Description | scientific article |
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author: Agnès Rötig Jean-Jacques Mourad Judith Favier Anne-Paule Gimenez-Roqueplo |
| Publication date | October 16, 2001 |
| Language | English |
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