首页> 外文OA文献 >Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene

【2h】

Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene

机译：莱伯先天性阿莫鲁病和色素性视网膜炎与外套类渗出性血管病是与面包屑同源物1（CRB1）基因的突变相关。

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
Hollander, Anneke I. den; Heckenlively, John R.; van den Born, L. Ingeborgh; de Kok, Yvette J. M.; van der Velde-Visser, Saskia D.; Kellner, Ulrich; Jurklies, Bernhard; van Schooneveld, Mary J.; Blankenagel, Anita; Rohrschneider, Klaus; Wissinger, Bernd; Cruysberg, Johan R. M.; Deutman, August F.; Brunner, Han G.; Apfelstedt-Sylla, Eckart; Hoyng, Carel B.; Cremers, Frans P. M.;
展开▼
作者单位

展开▼
年度 2001
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis [J] . José A. J. M. van den HurkPenny RashbassRonald RoepmanJason DavisKrysta E. J. VoesenekMaarten L. ArendsMarijke N. ZonneveldMarga H. G. van RoekelKaren CameronKlaus RohrschneiderJohn R. HeckenlivelyRobert K. KoenekoopCarel B. HoyngFrans P. M. CremersAnneke I. den Hollander Molecular vision . 2005,第2005期

机译：Crumbs同源2（CRB2）基因的表征及其在色素性视网膜炎和Leber先天性黑ur病中的作用分析
2. Mpdz null allele in an avian model of retinal degeneration and mutations in human leber congenital amaurosis and retinitis pigmentosa [J] . AliM., HockingP.M., McKibbinM., Investigative ophthalmology & visual science . 2011,第10期

机译：Mpdz无效等位基因在禽类视网膜变性和人类leber先天性黑睡病和色素性视网膜炎的突变模型中
3. Mpdz Null Allele in an Avian Model of Retinal Degeneration and Mutations in Human Leber Congenital Amaurosis and Retinitis Pigmentosa [J] . Manir Ali, Paul M. Hocking, Martin McKibbin, Investigative ophthalmology & visual science . 2011,第10期

机译：Mpdz无效等位基因在人类莱伯先天性无性和视网膜色素变性的视网膜变性和突变的禽类模型中。
4. Analysis of Retinal Degeneration in a Leber Congenital Amaurosis Mouse Model Using High Spatial Resolution MALDI-Imaging Mass Spectrometry [C] . David M. G. Anderson, Zsolt Ablonczy, Yiannis Koutalos, ASMS Conference on Mass Spectrometry and Allied Topics . 2016

机译：利用高空间分辨率MATDI成像质谱法分析LEBER先天性生物疲劳小鼠模型的视网膜变性
5. The Leber Congenital Amaurosis CEP290 Cat Model: Working Towards a Cure. [D] . Minella, Andrea Louise. 2017

机译：Leber先天性无门诊CEP290猫模型：正在努力治愈。
6. Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene [O] . Anneke I. den Hollander, John R. Heckenlively, L. Ingeborgh van den Born, 2001

机译：莱伯先天性阿莫鲁病和色素性视网膜炎与外套类渗出性血管病是与面包屑同源物1（CRB1）基因的突变相关。
7. Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene [O] . Hollander Anneke I. den, Heckenlively John R., van den Born L. Ingeborgh, 2001

机译：莱伯先天性阿莫鲁病和色素性视网膜炎与外套类渗出性血管病是与面包屑同源物1（CRB1）基因的突变相关。

Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene

著录项

引文网络

相似文献

相关主题

期刊订阅