Page last updated: 2024-10-20

thymine and Neurofibromatosis 2

thymine has been researched along with Neurofibromatosis 2 in 1 studies

Neurofibromatosis 2: An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bobest, M1
Tóth, C1
Gyurcsó, M1
Molnár, MJ1
Garzuly, F1

Other Studies

1 other study available for thymine and Neurofibromatosis 2

ArticleYear
[Nonsense mutation 193C>T of neurofibromatosis type 2--a neurosurgical challenge].
    Ideggyogyaszati szemle, 2007, Jan-20, Volume: 60, Issue:1-2

    Topics: Adolescent; Adult; Codon, Nonsense; Cytosine; Female; Genes, Neurofibromatosis 2; Humans; Magnetic R

2007