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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Detaylı Bibliyografya
Yayımlandı:Ann Neurol
Asıl Yazarlar: Svaren, John, Moran, John J., Wu, Xingyao, Zuccarino, Riccardo, Bacon, Chelsea, Bai, Yunhong, Ramesh, Raghu, Gutmann, Laurie, Anderson, Daniel M., Pavelec, Derek, Shy, Michael E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2019
Konular:
Article
Online Erişim: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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