In:
Clinical Pharmacology & Therapeutics, Wiley, Vol. 111, No. 4 ( 2022-04), p. 743-757
Abstract:
There are over 7,000 diseases that are individually rare, but collectively affect millions of people worldwide. They are very commonly neurologic single‐gene disorders. Recent advances in recombinant adeno‐associated virus vectors have enabled breakthroughs, including US Food and Drug Administration (FDA)–approved gene therapies for inherited retinal dystrophy due to RPE65 mutation and spinal muscular atrophy. A range of other gene therapies for rare neurologic diseases are at various stages of development. Future development of gene editing technologies promises further to broaden the potential for more patients with these disorders to benefit from innovative therapies.
Type of Medium:
Online Resource
ISSN:
0009-9236
,
1532-6535
Language:
English
Publisher:
Wiley
Publication Date:
2022
detail.hit.zdb_id:
2040184-X
SSG:
15,3
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