Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴疹样营养不良型大疱性表皮松解症家系的基因突变,为进
步开展基因诊断和基因治疗奠
基础。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴疹样营养不良型大疱性表皮松解症家系的基因突变,为进
步开展基因诊断和基因治疗奠
基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
:
上例句、词
分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类均由互联网资源自动,
分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
定一痒疹样营养不良型大疱性表皮松解症家系
基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类均由互源自动生成,部分未经过人工审核,其表达内容亦不代表本软件
观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异
双链法、SSCP法与异
双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上、词性分类均由互联网资
生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的突变,为进一步开展
断和
治疗奠定
础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源
法、SSCP法与异源
-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目鉴定一痒疹样营养不良型大疱性表皮松解症家
因
,为进一步开展
因诊断和
因治疗奠定
础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子
中ˇ异源双链法、SSCP法与异源双链-SSCP法检出
别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性类均由互联网资源自动生成,部
未经过人工审核,其表达内容亦不代表本软件
观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异
双链法、SSCP法与异
双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例、词性分类均由互联网
动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。