Screening for KCNJ2 mutations: The physician’s perspective
✍ Scribed by Extramiana, Fabrice
- Book ID
- 122366245
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 42 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1547-5271
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Neurofibromatosis 2 (NF2) is a genetic disorder caused by mutational inactivation of the __NF2__ gene and is characterized by bilateral vestibular schwannomas, spinal tumors, and other benign tumors of the nervous system. Previously, we found intragenic __NF2__ mutations in 99 of 188 un
Neurofibromatosiis type 2 (NF2) is a monogenic dominantly inherited disease that predisposes t o the development of tumors of the nervous system, particularly meningiomas and schwannomas. The gene which, when altered, causes NF2, is localized on chromosome 22 and has recently been identified. The NF