Clinicoradiologic data of familial cerebral cavernous malformation with age‐related disease burden

OBJECTIVE: Familial cerebral cavernous malformation (FCCM) is an autosomal dominant disease induced by loss‐of‐function mutations in three CCM genes, KRIT1, CCM2, and PDCD10. However, previous studies paid little attention to analyzing the radiologic features and age‐related disease burden according...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Seondeuk, Moon, Jangsup, Jung, Keun‐Hwa, Anh, Seon‐Jae, Lee, Han Sang, Jang, Yoonhyuk, Park, Kyung‐Il, Lee, Sang Kun, Chu, Kon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014009/
https://www.ncbi.nlm.nih.gov/pubmed/36629374
http://dx.doi.org/10.1002/acn3.51728

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014009/
https://www.ncbi.nlm.nih.gov/pubmed/36629374
http://dx.doi.org/10.1002/acn3.51728

Ejemplares similares