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ZNF408 gene
Known as:
FLJ12827
, ZINC FINGER PROTEIN 408
, ZNF408
National Institutes of Health
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Related topics
Related topics
2 relations
ZFPM1 wt Allele
Zinc Fingers
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Cohort study of genotype and clinical phenotype in 34 families with familial exudative vitreoretinopathy
Chunli Chen
,
Peiquan Zhao
,
Xiaorong Li
2020
Corpus ID: 219794449
Objective To observe and analyze the genotype and clinical phenotype in 34 families of familial exudative vitreoretinopathy…
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2019
2019
Microcornea, Posterior Megalolenticonus, Persistent Fetal Vasculature, and Coloboma Syndrome Associated With a New Mutation in ZNF408.
Geoffrey A. Weiner
,
E. Nudleman
Ophthalmic Surgery Lasers and Imaging Retina
2019
Corpus ID: 122332295
The authors report a case of a 6-week-old girl with microphthalmia, posterior lenticonus, persistent fetal vasculature, and…
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2018
2018
[Analysis of pathological mutation in a Chinese pedigree affected with familial exudative vitreoretinopathy].
Ning Su
,
Litao Qin
,
+4 authors
S. Liao
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2018
Corpus ID: 4844190
OBJECTIVE To detect potential mutation in a Chinese pedigree affected with familial exudative vitreoretinopathy (FEVR). METHODS…
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2017
2017
Mutations in LRP 5 , FZD 4 , TSPAN 12 , NDP , ZNF 408 , or KIF 11 Genes Account for 38 . 7 % of Chinese Patients With Familial Exudative Vitreoretinopathy
Feng-Qin Rao
,
Xue-Bi Cai
,
+6 authors
Zi‐Bing Jin
2017
Corpus ID: 120035
Citation: Rao F-Q, Cai X-B, Cheng F-F, et al. Mutations in LRP5, FZD4, TSPAN12, NDP, ZNF408, or KIF11 genes account for 38.7% of…
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2017
2017
Genetics Mutations in LRP 5 , FZD 4 , TSPAN 12 , NDP , ZNF 408 , or KIF 11 Genes Account for 38 . 7 % of Chinese Patients With Familial Exudative Vitreoretinopathy
Feng-Qin Rao
,
Xue-Bi Cai
,
+6 authors
Zi‐Bing Jin
2017
Corpus ID: 3613605
Citation: Rao F-Q, Cai X-B, Cheng F-F, et al. Mutations in LRP5, FZD4, TSPAN12, NDP, ZNF408, or KIF11 genes account for 38.7% of…
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2017
2017
Targeted NGS: an effective approach for molecular diagnosis of hereditary vitreoretinopathies
C. B. D. Roziers
,
Pierre-Raphaël Rothschild
,
+20 authors
S. Valleix
2017
Corpus ID: 80130382
Summary Hereditary vitreoretinopathies (VRPs), traditionally divided into the groups of exudative and degenerative VRPs…
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2012
2012
Combined Exome Sequencing And Linkage Analysis Reveals A Dominant-negative ZNF408 Mutation Causing Familial Exudative Vitreoretinopathy
R. Collin
,
K. Nikopoulos
,
+7 authors
F. Cremers
2012
Corpus ID: 82255206
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