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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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| Publicado no: | Chin Med J (Engl) |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2021
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| Assuntos: | |
| Acesso em linha: | 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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