Identification of two sporadically derived mutations in the Von Hippel-Lindau gene

Hum Mutat. 1996;7(2):185. doi: 10.1002/(SICI)1098-1004(1996)7:2<185::AID-HUMU22>3.0.CO;2-Y.

Authors

R L Martin¹, I Walpole, J Goldblatt

Affiliation

¹ Princess Margaret Hospital for Children, Perth, Australia.

PMID: 8829648
DOI: 10.1002/(SICI)1098-1004(1996)7:2<185::AID-HUMU22>3.0.CO;2-Y

No abstract available

MeSH terms

Genes, Tumor Suppressor / genetics*
Heterozygote
Humans
Phenotype
Point Mutation*
von Hippel-Lindau Disease / genetics*