Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development

BACKGROUND/AIM: The number of reports on the role of tubulin gene mutations ( TUBA1A, TUBB2B, and TUBB3 ) in etiology of malformations of cortical development has peaked in recent years. We aimed to determine tubulin gene defects on a patient population with simple and complex malformations of corti...

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Detalles Bibliográficos
Autores principales: AKSEL KILIÇARSLAN, Özge, ATAMAN, Esra, GÜRSOY, Semra, GÜRBÜZ, Gürkan, ÜNALP, Aycan, GENÇPINAR, Pınar, OLGAÇ DÜNDAR, Nihal, EDİZER, Selvinaz, ÜLGENALP, Ayfer, GİRAY BOZKAYA, Özlem
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/PMC7605093/
https://www.ncbi.nlm.nih.gov/pubmed/32718119
http://dx.doi.org/10.3906/sag-1901-170

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7605093/
https://www.ncbi.nlm.nih.gov/pubmed/32718119
http://dx.doi.org/10.3906/sag-1901-170

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