Found: 6
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Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L.
- Published in:
- Human Genetics, 2005, v. 116, n. 3, p. 222, doi. 10.1007/s00439-004-1218-3
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- Publication type:
- Article
Progress in treatment of Charcot?Marie?Tooth disease.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2017, v. 17, n. 8, p. 566, doi. 10.3969/j.issn.1672-6731.2017.08.003
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- Publication type:
- Article
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.
- Published in:
- 2019
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- Publication type:
- journal article
Heterozygous Seryl‐tRNA Synthetase 1 Variants Cause Charcot–Marie–Tooth Disease.
- Published in:
- Annals of Neurology, 2023, v. 93, n. 2, p. 244, doi. 10.1002/ana.26501
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- Publication type:
- Article
Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy Study.
- Published in:
- Movement Disorders, 2022, v. 37, n. 9, p. 1807, doi. 10.1002/mds.29180
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- Publication type:
- Article
The progress in diagnosis and treatment of transthyretin amyloid polyneuropathy.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 6, p. 430, doi. 10.3969/j.issn.1672-6731.2021.06.002
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- Publication type:
- Article