Novel mutations in HTRA1 ‐related cerebral small vessel disease and comparison with CADASIL

OBJECTIVE: There is evidence showing both heterozygous HTRA1 and homozygous HTRA1 mutations as causal for familial cerebral small vessel disease (CSVD). The clinical and neuroimaging signs of heterozygous HTRA1‐related CSVD can mimic cerebral autosomal dominant arteriopathy with subcortical infarcts...

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Detalles Bibliográficos
Autores principales: Zhang, Chen, Zheng, Honghua, Li, Xin, Li, Shaowu, Li, Wei, Wang, Ziwei, Niu, Songtao, Wang, Xingao, Zhang, Zaiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9539375/
https://www.ncbi.nlm.nih.gov/pubmed/36047879
http://dx.doi.org/10.1002/acn3.51654

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9539375/
https://www.ncbi.nlm.nih.gov/pubmed/36047879
http://dx.doi.org/10.1002/acn3.51654

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