Concepedia

MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours

Joakim Crona, Rajani Maharjan, Alberto Delgado Verdugo, Peter Stålberg, Per Hellman, Peyman Björklund

Familial Cancer · 2013 · 11 citations · 23 references

DOI

Concepts

References

23

Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene

Farida Latif, Kálmán Tory, James R. Gnarra et al. · Science · 1993 · 3K citations

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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

Lois M. Mulligan, John B. Kwok, Catherine S. Healey et al. · Nature · 1993 · 2K citations

, , +16

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

, , +16

Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients

Margaret R. Wallace, Douglas A. Marchuk, Lone B. Andersen et al. · Science · 1990 · 1.5K citations

, , +10

Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma

Dewi Astuti, Farida Latif, Ashraf Dallol et al. · The American Journal of Human Genetics · 2001 · 1.1K citations · Full text

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