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Schwann Cell Transcript Biomarkers for Hereditary Neuropathy Skin Biopsies
OBJECTIVE: Charcot-Marie-Tooth disease (CMT) is most commonly caused by duplication of a chromosomal segment surrounding Peripheral Myelin Protein 22, or PMP22 gene, which is classified as CMT1A. Several candidate therapies reduce Pmp22 mRNA levels in CMT1A rodent models, but development of biomarke...
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| 出版年: | Ann Neurol |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7050273/ https://ncbi.nlm.nih.gov/pubmed/30945774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.25480 |
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