Gene Therapies for Monogenic Autism Spectrum Disorders

被引:12
|
作者
Weuring, Wout [1 ]
Geerligs, Jeroen [1 ]
Koeleman, Bobby P. C. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Genet, NL-3584 Utrecht, Netherlands
关键词
ASD; gene therapy; gene edit; RNA therapy; epilepsy; gene replacement; gene delivery; CRISPR/Cas9; noncoding RNA; ANGELMAN SYNDROME; RNA; EXPRESSION; DELIVERY; DNA;
D O I
10.3390/genes12111667
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Novel genome editing and transient gene therapies have been developed the past ten years, resulting in the first in-human clinical trials for monogenic disorders. Syndromic autism spectrum disorders can be caused by mutations in a single gene. Given the monogenic aspect and severity of syndromic ASD, it is an ideal candidate for gene therapies. Here, we selected 11 monogenic ASD syndromes, validated by animal models, and reviewed current gene therapies for each syndrome. Given the wide variety and novelty of some forms of gene therapy, the best possible option must be decided based on the gene and mutation.
引用
收藏
页数:9
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