Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations-Reference-Cited by-同舟云学术

Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations

Published:2021-08 Issue:8 Volume:29 Page:2441-2455
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Dulla Kalyan,Slijkerman Ralph^ORCID,van Diepen Hester C.,Albert Silvia^ORCID,Dona Margo^ORCID,Beumer Wouter^ORCID,Turunen Janne J.^ORCID,Chan Hee Lam,Schulkens Iris A.^ORCID,Vorthoren Lars,den Besten Cathaline,Buil Levi,Schmidt Iris,Miao Jiayi,Venselaar Hanka,Zang Jingjing,Neuhauss Stephan C.F.^ORCID,Peters Theo^ORCID,Broekman Sanne,Pennings Ronald^ORCID,Kremer Hannie^ORCID,Platenburg Gerard^ORCID,Adamson Peter,de Vrieze Erik^ORCID,van Wijk Erwin^ORCID

Funder

ZonMw

Foundation Fighting Blindness Inc

Publisher

Elsevier BV

Subject

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

Reference54 articles.

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2. Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa;McGee;J. Med. Genet.,2010

3. Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss;Rivolta;Am. J. Hum. Genet.,2000

4. USH2A mutation analysis in 70 Dutch families with Usher syndrome type II;Pennings;Hum. Mutat.,2004

5. The USH2A c.2299delG mutation: dating its common origin in a Southern European population;Aller;Eur. J. Hum. Genet.,2010

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