外显子
基因
遗传学
突变
疾病
帕金森病
退行性疾病
生物
中枢神经系统疾病
医学
神经科学
内科学
作者
Süleyman Güler,Tuğçe Gül,Şükran Güler,Maja C. Haerle,A. Nazlı Başak
摘要
Patients with mutations in DJ-1 have early-onset Parkinson's disease and slow progression. Here we describe a Turkish family with a large deletion in the neighboring genes DJ-1 (del exons 1-5) and TNFRSF9 (del exons 1-6), raising the question if TNFRSF9 is a possible disease modifier.
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