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Since identification of the\n                    <jats:italic>NF2<\/jats:italic>\n                    gene more than a decade ago, a large body of information has been collected on the nature and consequences of these alterations in patients with NF2 and in individuals in whom sporadic tumors associated with NF2 develop. The catalog of mutations identified thus far has facilitated extensive genetic analysis, including studies of patients with mosaicism and phenotype\u2013genotype correlations, and has also led to experiments that have begun to unravel the molecular biology of the\n                    <jats:italic>NF2<\/jats:italic>\n                    gene and its role in tumorigenesis. The authors describe some of the most significant findings in\n                    <jats:italic>NF2<\/jats:italic>\n                    genetics and biology over the last decade.\n                  <\/jats:p>","DOI":"10.3171\/foc.2005.19.5.7","type":"journal-article","created":{"date-parts":[[2008,1,24]],"date-time":"2008-01-24T07:13:18Z","timestamp":1201158798000},"page":"1-5","source":"Crossref","is-referenced-by-count":14,"title":["Role of the neurofibromatosis Type 2 gene in the development of tumors of the nervous system"],"prefix":"10.3171","volume":"19","author":[{"given":"Martin H.","family":"Ruttledge","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guy 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