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Editorial Comment to p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens)

机译：对p.Leu636pro突变的编辑评论与囊性纤维化跨膜传导调节因子相关的疾病（先天性双侧输精管缺如）有关

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作者
Castaldo Giuseppe; Amato Felice;
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年度 2015
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正文语种 eng
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1. Comprehensive and Rapid Genotyping of Mutations and Haplotypes in Congenital Bilateral Absence of the Vas Deferens and Other Cystic Fibrosis Transmembrane Conductance Regulator-Related Disorders [J] . Corinne Bareil* Caroline Guittard* Jean-Pierre Altieri* Carine Templin* Mireille Claustres* and Marie des Georges The Journal of Molecular Diagnostics . 2007,第5期

机译：对先天性双侧无输精管和其他囊性纤维化跨膜电导调节剂相关疾病的突变和单倍型进行全面，快速的基因分型。
2. Comprehensive and rapid genotyping of mutations and haplotypes in congenital bilateral absence of the vas deferens and other cystic fibrosis transmembrane conductance regulator-related disorders. [J] . Bareil C, Guittard C, Altieri JP, The Journal of molecular diagnostics: JMD . 2007,第5期

机译：先天性双侧无输精管和其他囊性纤维化跨膜电导调节剂相关疾病的突变和单倍型的综合快速基因分型。
3. The detection and significance of cystic fibrosis transmembrane conductance regulator gene promoter mutations in Chinese patients with congenital bilateral absence of the vas deferens [J] . Bai Song, Du Qiang, Liu Xiaoliang, Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function . 2018,第期

机译：囊性纤维化跨膜电导调节剂基因启动子突变在中国先天性双侧缺失的患者缺失的检测及意义
4. Cystic fibrosis transmembrane conductance regulator gene mutations cause 'black' pigment gallstone formation: new insights from mouse models and implications for therapeutic interventions in cystic fibrosis [C] . A. L. BRODERICK, H. WITTENBURG, M. A. LYONS, Falk Symposium . 2004

机译：囊性纤维化跨膜电导调节剂基因突变引起'黑色'颜料胆结石形成：来自小鼠模型的新见解，以及对囊性纤维化治疗干预的影响
5. Consequences of mutation and variable expression on functions of the cystic fibrosis transmembrane conductance regulator. [D] . Fulmer-Smentek, Stephanie Borland. 1998

机译：突变和可变表达对囊性纤维化跨膜电导调节器功能的影响。
6. Comprehensive and Rapid Genotyping of Mutations and Haplotypes in Congenital Bilateral Absence of the Vas Deferens and Other Cystic Fibrosis Transmembrane Conductance Regulator-Related Disorders [O] . Corinne Bareil, Caroline Guittard, Jean-Pierre Altieri, 2007

机译：对先天性双侧无输精管和其他囊性纤维化跨膜电导调节剂相关疾病的突变和单倍型进行全面快速的基因分型。
7. Editorial Comment to p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens) [O] . Giuseppe Castaldo, Felice Amato 2015

机译：编辑评论对P.Leu636Pro突变与囊性纤维化跨膜电导调节器相关疾病有关（先天性双侧没有VAS推送）

Editorial Comment to p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens)

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