Sainio, M

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