Niemann, S <br/><br/>
Mutations in SDHC cause autosomal dominant paraganglioma, type 3.  [electronic resource] 

 -  Nature genetics  Nov 2000 
 - 268-70 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/81551  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 1--genetics<br/>DNA Mutational Analysis<br/>DNA, Complementary--genetics<br/>Electron Transport Complex II<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Male<br/>Membrane Proteins--deficiency<br/>Mitochondria--enzymology<br/>Molecular Sequence Data<br/>Multienzyme Complexes--chemistry<br/>Mutagenesis, Site-Directed<br/>Neoplastic Syndromes, Hereditary--enzymology<br/>Oxidoreductases--chemistry<br/>Paraganglioma--classification<br/>Pedigree<br/>Protein Subunits<br/>Succinate Dehydrogenase--chemistry