載入...
How common are single gene mutations as a cause for lacunar stroke?: A targeted gene panel study
OBJECTIVES: To determine the frequency of rare and pertinent disease-causing variants in small vessel disease (SVD)-associated genes (such as NOTCH3, HTRA1, COL4A1, COL4A2, FOXC1, TREX1, and GLA) in cerebral SVD, we performed targeted gene sequencing in 950 patients with younger-onset apparently spo...
Na minha lista:
| 發表在: | Neurology |
|---|---|
| Main Authors: | , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Lippincott Williams & Wilkins
2019
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6913325/ https://ncbi.nlm.nih.gov/pubmed/31719132 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000008544 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|