Cas9-induced single cut enables highly efficient and template-free repair of a muscular dystrophy causing founder mutation
Author:
Publisher
Elsevier BV
Subject
Drug Discovery,Molecular Medicine
Reference59 articles.
1. Calpainopathy—a survey of mutations and polymorphisms;Richard;Am. J. Hum. Genet.,1999
2. Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes;Piluso;J. Med. Genet.,2005
3. Prevalence of the 550delA mutation in calpainopathy (LGMD 2A) in Croatia;Canki-Klain;Am. J. Med. Genet. A,2004
4. Disease progression and mutation pattern in a large cohort of LGMD R1/LGMD 2A patients from India;Ganaraja;Glob. Med. Genet.,2021
5. May 10[Updated 2017 Aug 3];Angelini,2005
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