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Hepatitis C Virus Induced Sjogren Syndrome - Clinical and Imaging Features
Currently incurable, Charcot-Marie-Tooth (CMT) disease is the most commonly inherited neurological disorder, which affects a small percentage of the population. The most common cause of CMT is the duplication of a region on the short arm of chromosome 17, which includes the gene PMP22. We report a t...
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| I publikationen: | Curr Health Sci J |
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| Huvudupphovsmän: | , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Medical University Publishing House Craiova
2017
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6286722/ https://ncbi.nlm.nih.gov/pubmed/30595859 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12865/CHSJ.43.01.12 |
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