CRISPR/Cas9 in zebrafish: An attractive model for FBN1 genetic defects in humans
Author:
Affiliation:
1. Medical School of Chinese PLA Beijing China
2. Clinical Biobank Center, the Medical Innovation Research Division Chinese PLA General Hospital Beijing China
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1775
Reference67 articles.
1. Genome editing using CRISPR/Cas9-based knock-in approaches in zebrafish
2. Homozygous and compound heterozygous mutations in theFBN1gene: unexpected findings in molecular diagnosis of Marfan syndrome
3. Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)
4. Shprintzen-Goldberg Syndrome: A Rare Disorder
5. A glance at genome editing with CRISPR–Cas9 technology
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