| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1021880554 |
| P356 | DOI | 10.1186/S10194-016-0646-5 |
| P932 | PMC publication ID | 4875019 |
| P698 | PubMed publication ID | 27206574 |
| P2093 | author name string | Wei Wang | |
| Dan He | |||
| Xiang Luo | |||
| Xuefei Li | |||
| Zheng Hu | |||
| Zhiyuan Yu | |||
| Daiqi Chen | |||
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| High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). | Q54474722 | ||
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| Diagnostic strategies in CADASIL | Q73563077 | ||
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| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P304 | page(s) | 55 | |
| P577 | publication date | 2016-05-20 | |
| P1433 | published in | The journal of headache and pain : official journal of the Italian Society for the Study of Headaches | Q26842211 |
| P1476 | title | The comparisons of phenotype and genotype between CADASIL and CADASIL-like patients and population-specific evaluation of CADASIL scale in China | |
| P478 | volume | 17 |
| Q38663098 | CADASIL: Treatment and Management Options. |
| Q91671885 | First Report of a pCys194Arg Notch 3 Mutation in a Romanian CADASIL Patient with Transient Ischemic Attacks and Patent Foramen Ovale - Case Report and Brief Review |
| Q89980521 | Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report |
| Q37436780 | Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients. |
| Q57476259 | The role of clinical and neuroimaging features in the diagnosis of CADASIL |
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