夏寅 Merlin蛋白与Ⅱ型神经纤维瘤病 -国际耳鼻咽喉头颈外科杂志2009,33(4) Ⅱ型神经纤维瘤病(neurofibromatosis type 2,NF2)是常染色体显性遗传疾病,NF2基因突变是其发病的主要分子机制,其编码蛋白产物merlin蛋白的 失活...
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Biallelic inactivation of the NF2 gene was detected in 36% of meningiomas.
NF 2双等位基因钝化可在36%的脑膜瘤中检测到。
The method to implement multimedia database system NHMDB based on NF2 model is described in the paper.
本文论述了基于NF2模型实现多介质数据库系统NHMDB的方法。
Among the monosomy 22 cases, no additional NF2 mutations could be identified in 35% (17 out of 49) of tumors.
在单体22病例中，35%的肿瘤中(49例中有17例)没有检测到多余的NF 2突变。
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