Mild familial neurofibromatosis 2 associates with expression of merlin with altered COOH-terminus. [electronic resource]
- Neurology Mar 2000
- 1132-8 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0028-3878
10.1212/wnl.54.5.1132 doi
Alleles Exons Genes, Neurofibromatosis 2--genetics Humans Immunoblotting Loss of Heterozygosity Membrane Proteins--analysis Mutation--genetics Neurofibromatosis 2--genetics Neurofibromin 2 Pedigree Phenotype