HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome
Nature Genetics2002Vol. 32(4), pp. 676–680
Citations Over TimeTop 10% of 2002 papers
John D. Carpten, Christiane M. Robbins, Andrea Villablanca, Lars Forsberg, Silvano Presciuttini, Joan E. Bailey‐Wilson, William F. Simonds, Elizabeth M. Gillanders, Ann Kennedy, J.D. Chen, Sunita Agarwal, Raman Sood, Matthew P. Jones, Tracy Moses, Carola J. Haven, David Petillo, Poloko D. Leotlela, Brian Harding, Donald P. Cameron, A. A. J. Pannett, Anders Höög, Hunter Heath, Laura James‐Newton, Bruce Robinson, Richard J. Zarbo, Branca Cavaco, W Wassif, Nancy D. Perrier, Irving B. Rosen, Ulf Kristoffersson, Peter D. Turnpenny, L.‐O. Farnebo, G. M. Besser, Charles E. Jackson, Hans Morreau, Jeffrey M. Trent, Rajesh V. Thakker, Stephen J. Marx, Bin Tean Teh, Catharina Larsson, Maurine R. Hobbs
Related Papers
- → Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan(1996)502 cited
- → Differences between germline and somatic mutation rates in humans and mice(2017)431 cited
- → The mutational landscape of human somatic and germline cells(2022)13 cited
- → Germline mutations in the Von Hippel‐Lindau disease (VHL) gene in families from North America, Europe, and Japan(1996)42 cited
- → 28. Identification of TP53 germline variants in pediatric patients undergoing tumor testing(2022)