Allele-selective CRISPR deletion as a therapy for ACTA1 congenital myopathy

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Authors: Therapeutic Innovation Australia
Cited by: 0

Fields of Study & Subjects

CRISPR and Genetic Engineering Muscle Physiology and Disorders Neurogenetic and Muscular Disorders Research

Publication details

Journal / source
Therapeutic Innovation Australia
Publication date
17 February 2026
Language
EN