Models for the development of tumours in neurofibromatosis 2
Neurofibromatosis 2 (NF2) is a rare genetic disease that affects approximately 1 in 40000 people, some of the characteristic features of this disease include the onset of multiple tumours on the cranial and spinal nerves, juvenile cataracts and hearing loss. Almost all affected individuals develo...
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Format: | Others |
Language: | English |
Published: |
2009
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Online Access: | http://hdl.handle.net/2429/11019 |