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HTRA1-related autosomal dominant cerebral small vessel disease
BACKGROUND: Homozygous or compound heterozygous mutations in high temperature requirement serine peptidase A1 (HTRA1) gene are responsible for cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL). Recently, increasing evidence has shown that heterozyg...
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| Pubblicato in: | Chin Med J (Engl) |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Lippincott Williams & Wilkins
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7817319/ https://ncbi.nlm.nih.gov/pubmed/33109952 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/CM9.0000000000001176 |
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