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Promoting identification of amyotrophic lateral sclerosis based on label‐free plasma spectroscopy.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 10, p. 2010, doi. 10.1002/acn3.51194
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- Article
Identification of SLC20A2 deletions in patients with primary familial brain calcification.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 1, p. 53, doi. 10.1111/cge.13540
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- Publication type:
- Article
Prognostic analysis of amyotrophic lateral sclerosis based on clinical features and plasma surface‐enhanced Raman spectroscopy.
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- Journal of Biophotonics, 2019, v. 12, n. 8, p. N.PAG, doi. 10.1002/jbio.201900012
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- Article
Correction to: Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies.
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- 2020
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- Publication type:
- Correction Notice
Whole Exome Sequencing Identifies Two Novel Mutations in the Reticulon 4–Interacting Protein 1 Gene in a Chinese Family with Autosomal Recessive Optic Neuropathies.
- Published in:
- Journal of Molecular Neuroscience, 2019, v. 68, n. 4, p. 640, doi. 10.1007/s12031-019-01319-7
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- Publication type:
- Article
Spectrum of SLC20A2, PDGFRB, PDGFB, and XPR1 mutations in a large cohort of patients with primary familial brain calcification.
- Published in:
- Human Mutation, 2019, v. 40, n. 4, p. 392, doi. 10.1002/humu.23703
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- Article