NOTCH3 Variants in Patients with Suspected CADASIL

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarctions and leukoencephalopathy (CADASIL) is the most common hereditary form of cerebral small vessel disease. It is clinically, radiologically, and genetically heterogeneous and is caused by NOTCH3 mutations. METHODS: In this...

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Detalles Bibliográficos
Autores principales: Gorukmez, Orhan, Gorukmez, Ozlem, Topak, Ali, Seferoglu, Meral, Sivaci, Ali O., Ali, Asuman, Tepe, Nermin, Kabay, Sibel C., Taskapılıoglu, Ozlem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645240/
https://www.ncbi.nlm.nih.gov/pubmed/37970308
http://dx.doi.org/10.4103/aian.aian_989_22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645240/
https://www.ncbi.nlm.nih.gov/pubmed/37970308
http://dx.doi.org/10.4103/aian.aian_989_22

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