Mutations in SDHC cause autosomal dominant paraganglioma, type 3

Mutations in <i>SDHD</i> , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma

Bora E. Baysal, Robert E. Ferrell, Joan E. Willett-Brozick et al. · Science · 2000 · 1.6K citations

Life Sciences, Genetics, Molecular Genetics +16

PROSPECTIVE RANDOMISED TRIAL OF EARLY DIETARY PROTEIN RESTRICTION IN CHRONIC RENAL FAILURE

Johan Rosman, PietM. Ter Wee, Sijtze Meijer Truus et al. · The Lancet · 1984 · 555 citations

Agriculture, Nephrology, Nutritional Sciences +9

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

Peter Heutink, Andel G. L. van der Mey, Lodewijk A. Sandkuijl et al. · Human Molecular Genetics · 1992 · 217 citations

Life Sciences, Genetics, Otolaryngology +10

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

Edwin C.M. Mariman, Sylvia E. C. van Beersum, Cor W. R. J. Cremers et al. · Human Genetics · 1995 · 140 citations

Life Sciences, Genetics, Molecular Genetics +17

Cytochrome b in human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the components in liver mitochondria and chromosome assignment of the genes for the large (SDHC) and small (SDHD) subunits to 1q21 and 11q23

Hiroko Hirawake, Masafumi Taniwaki, Akiko Tamura et al. · Cytogenetics and Cell Genetics · 2008 · 63 citations

Life Sciences, Biochemistry, Molecular Biology +12