000 01481 a2200433 4500
005 20250513223346.0
264 0 _c20001213
008 200012s 0 0 eng d
022 _a1061-4036
024 7 _a10.1038/81551
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNiemann, S
245 0 0 _aMutations in SDHC cause autosomal dominant paraganglioma, type 3.
_h[electronic resource]
260 _bNature genetics
_cNov 2000
300 _a268-70 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChromosomes, Human, Pair 1
_xgenetics
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDNA, Complementary
_xgenetics
650 0 4 _aElectron Transport Complex II
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMembrane Proteins
_xdeficiency
650 0 4 _aMitochondria
_xenzymology
650 0 4 _aMolecular Sequence Data
650 0 4 _aMultienzyme Complexes
_xchemistry
650 0 4 _aMutagenesis, Site-Directed
650 0 4 _aNeoplastic Syndromes, Hereditary
_xenzymology
650 0 4 _aOxidoreductases
_xchemistry
650 0 4 _aParaganglioma
_xclassification
650 0 4 _aPedigree
650 0 4 _aProtein Subunits
650 0 4 _aSuccinate Dehydrogenase
_xchemistry
700 1 _aMüller, U
773 0 _tNature genetics
_gvol. 26
_gno. 3
_gp. 268-70
856 4 0 _uhttps://doi.org/10.1038/81551
_zAvailable from publisher's website
999 _c11004987
_d11004987