TY  - GEN
AU  - Niemann,S
AU  - Müller,U
TI  - Mutations in SDHC cause autosomal dominant paraganglioma, type 3
SN  - 1061-4036
PY  - 2000///1213
KW  - Chromosomes, Human, Pair 1
KW  - genetics
KW  - DNA Mutational Analysis
KW  - DNA, Complementary
KW  - Electron Transport Complex II
KW  - Female
KW  - Genes, Dominant
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - deficiency
KW  - Mitochondria
KW  - enzymology
KW  - Molecular Sequence Data
KW  - Multienzyme Complexes
KW  - chemistry
KW  - Mutagenesis, Site-Directed
KW  - Neoplastic Syndromes, Hereditary
KW  - Oxidoreductases
KW  - Paraganglioma
KW  - classification
KW  - Pedigree
KW  - Protein Subunits
KW  - Succinate Dehydrogenase
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/81551
ER  -