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Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A
OBJECTIVE: Development of biomarkers for Charcot‐Marie‐Tooth (CMT) disease is critical for implementing effective clinical trials. The most common form of CMT, type 1A, is caused by a genomic duplication surrounding the PMP22 gene. A recent report (Neurology 2018;90:e518–3524) showed elevation of ne...
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| Gepubliceerd in: | Ann Clin Transl Neurol |
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| Hoofdauteurs: | , , , , , , , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2019
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6952315/ https://ncbi.nlm.nih.gov/pubmed/31833243 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50965 |
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