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The frequency of the delta F508 mutation in the cystic fibrosis genes of 71 unrelated South African cystic fibrosis patients

机译：71例无关的南非囊性纤维化患者囊性纤维化基因中ΔF508突变的频率

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Herbert J.S.; Retief A.E.;
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年度 1992
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正文语种 en
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1. The Cystic Fibrosis-causing Mutation ΔF508 Affects Multiple Steps in Cystic Fibrosis Transmembrane Conductance Regulator Biogenesis [J] . Patrick Thibodeau, John Richardson, Wei Wang, The Journal of biological chemistry . 2010,第期

机译：囊性纤维化导致突变ΔF508影响囊性纤维化跨膜电导调节剂生物发生的多个步骤
2. Frequency of Genotype With ΔF508 Mutation in CFTR Gene Among Iranian Cystic Fibrosis Patients With Pancreatic Insufficiency [J] . Ahmad Khodadad, * Elaheh Elahi, Setareh Sadat Bani Hassani, Iranian journal of pediatrics . 2015,第6期

机译：伊朗囊性纤维化胰腺功能不全患者CFTR基因中带有ΔF508突变的基因型频率
3. Chemiluminescent hybridization-ligation assays for delta F508 and delta I507 cystic fibrosis mutations. [J] . J C Arruda, P Dwivedi, R A Martinelli Clinical Chemistry: Journal of the American Association for Clinical Chemists . 1996,第1期

机译：δF508和δI507囊性纤维化突变的化学发光杂交-连接测定。
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. Detection of Cystic Fibrosis Transmembrane Conductance Regulator DeltaF508 Gene Mutation Using a Paper-Based Nucleic Acid Hybridization Assay and a Smartphone Camera [D] . Malhotra, Karan. 2018

机译：纸质核酸杂交检测和智能手机相机检测囊性纤维化跨膜电导调节剂DeltaF508基因突变
6. Cystic fibrosis in the Basque country: high frequency of mutation delta F508 in patients of Basque origin. [O] . T Casals, C Vázquez, C Lázaro, 1992

机译：巴斯克地区囊性纤维化：起源于巴斯克地区的患者突变三角洲F508的发生频率较高。
7. The frequency of the delta F508 mutation in the cystic fibrosis genes of 71 unrelated South African cystic fibrosis patients [O] . Herbert J.S., Retief A.E. 1992

机译：71例无关的南非囊性纤维化患者囊性纤维化基因中ΔF508突变的频率

The frequency of the delta F508 mutation in the cystic fibrosis genes of 71 unrelated South African cystic fibrosis patients

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