No abstract available
MeSH terms
-
Adolescent
-
Chromosomes, Human, Pair 22 / genetics*
-
Genes, Neurofibromatosis 2 / genetics*
-
Hereditary Sensory and Motor Neuropathy / genetics
-
Humans
-
Male
-
Mutation*
-
Neurilemmoma / genetics
-
Neurofibromatosis 2 / genetics*