首页>
外国专利>
PROBE FOR DIAGNOSIS OF MARFAN'S SYNDROME AND METHOD OF SCREENING WITH THE PROBE
PROBE FOR DIAGNOSIS OF MARFAN'S SYNDROME AND METHOD OF SCREENING WITH THE PROBE
展开▼
机译:马凡氏综合征的诊断探针和筛查方法
展开▼
页面导航
摘要
著录项
相似文献
摘要
The purpose of this invention is to provide a probe for diagnosis of Marfan syndrome, which enables early diagnosis of Marfan syndrome, and to provide a method for screening using said probe. The invention is a probe for a Marfan Syndrome characterized by using a nucleic acid comprising following (a) or (b); (a) a nucleic acid comprising a base sequence represented by base numbers 1-180000 shown in SEQ ID No. 1 of the sequence listing, or (b) a nucleic acid in which a part of the base sequence of said base numbers 1-180000 is deleted, substituted or added, and having 80% homology with said base sequence.
展开▼
机译:本发明的目的是提供用于诊断马凡氏综合症的探针,其能够早期诊断马凡氏综合症,并提供使用所述探针进行筛选的方法。本发明是用于马凡氏综合症的探针,其特征在于使用包含以下(a)或(b)的核酸。(a)一种核酸,其包含由序列表的SEQ ID No.1所示的碱基编号1-180000表示的碱基序列,或(b)一种核酸,其中所述碱基编号1-180000的部分碱基序列被缺失,取代或添加,并且与所述碱基序列具有80%的同源性。
展开▼