Found: 6
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Early onset hereditary neuronopathies: an update on non-5q motor neuron diseases.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 3, p. 806, doi. 10.1093/brain/awac452
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- Article
Publisher Correction: Necroptosis mediates myofibre death in dystrophin-deficient mice.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06636-w
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- Publication type:
- Article
Necroptosis mediates myofibre death in dystrophin-deficient mice.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06057-9
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- Publication type:
- Article
GGPS1-associated muscular dystrophy with and without hearing loss.
- Published in:
- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 9, p. 1465, doi. 10.1002/acn3.51633
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- Article
Recessive variants in COL25A1 gene as novel cause of arthrogryposis multiplex congenita with ocular congenital cranial dysinnervation disorder.
- Published in:
- Human Mutation, 2022, v. 43, n. 4, p. 487, doi. 10.1002/humu.24333
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- Publication type:
- Article
Transiently expressed CRISPR/Cas9 induces wild-type dystrophin in vitro in DMD patient myoblasts carrying duplications.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-07671-w
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- Publication type:
- Article