Genome-wide identification of Chiari malformation type I associated candidate genes and chromosomal variations

Chiari malformation type I (CMI) is a brain malformation that is characterized by herniation of the cerebellum into the spinal canal. Chiari malformation type I is highly heterogeneous; therefore, an accurate explanation of the pathogenesis of the disease is often not possible. Although some studies...

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Detalles Bibliográficos
Autores principales: AVŞAR, Timuçin, ÇALIŞ, Şeyma, YILMAZ, Baran, DEMİRCİ OTLUOĞLU, Gülden, HOLYAVKİN, Can, KILIÇ, Türker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759189/
https://www.ncbi.nlm.nih.gov/pubmed/33402871
http://dx.doi.org/10.3906/biy-2009-19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759189/
https://www.ncbi.nlm.nih.gov/pubmed/33402871
http://dx.doi.org/10.3906/biy-2009-19

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