CRISPR-Cas9 correction of OPA1 c.1334G>A: p.R445H restores mitochondrial homeostasis in dominant optic atrophy patient-derived iPSCs: Molecular Therapy - Nucleic Acids
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Understanding the molecular basis and pathogenesis of hereditary
Drosophila model to clarify the pathological significance of OPA1
PDF) Modelling autosomal dominant optic atrophy associated with
Antioxidants, Free Full-Text
Characterisation of a novel OPA1 splice variant resulting in
CRISPR/Cas9 therapeutics: progress and prospects
OPA1 Mutation and Late‐Onset Cardiomyopathy: Mitochondrial
CRISPR/Cas9-mediated A4GALT suppression rescues Fabry disease
JCM, Free Full-Text
Understanding the molecular basis and pathogenesis of hereditary
Drosophila model to clarify the pathological significance of OPA1
JCM, Free Full-Text
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