CRISPR/Cas9-Induced (CTG⋅CAG) n Repeat Instability in the Myotonic Dystrophy Type 1 Locus: Implications for Therapeutic Genome Editing-Reference-Cited by-同舟云学术

CRISPR/Cas9-Induced (CTG⋅CAG) n Repeat Instability in the Myotonic Dystrophy Type 1 Locus: Implications for Therapeutic Genome Editing

Published:2017-01 Issue:1 Volume:25 Page:24-43
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

van Agtmaal Ellen L.,André Laurène M.,Willemse Marieke,Cumming Sarah A.,van Kessel Ingeborg D.G.,van den Broek Walther J.A.A.,Gourdon Geneviève,Furling Denis,Mouly Vincent,Monckton Darren G.,Wansink Derick G.,Wieringa Bé

Funder

ZonMw

Prinses Beatrix Spierfonds

Stichting Spieren voor Spieren

Radboudumc

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

Reference83 articles.

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3. Expanding complexity in myotonic dystrophy;Groenen;BioEssays,1998

4. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992

5. Myotonic dystrophy mutation: an unstable CTG repeat in the 3′ untranslated region of the gene;Mahadevan;Science,1992

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