Mutations in SDHC cause autosomal dominant paraganglioma, type 3. [electronic resource]
Producer: 20001213Description: 268-70 p. digitalISSN:- 1061-4036
- Chromosomes, Human, Pair 1 -- genetics
- DNA Mutational Analysis
- DNA, Complementary -- genetics
- Electron Transport Complex II
- Female
- Genes, Dominant
- Humans
- Male
- Membrane Proteins -- deficiency
- Mitochondria -- enzymology
- Molecular Sequence Data
- Multienzyme Complexes -- chemistry
- Mutagenesis, Site-Directed
- Neoplastic Syndromes, Hereditary -- enzymology
- Oxidoreductases -- chemistry
- Paraganglioma -- classification
- Pedigree
- Protein Subunits
- Succinate Dehydrogenase -- chemistry
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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