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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...
Kaydedildi:
| Yayımlandı: | Turk J Med Sci |
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| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Scientific and Technological Research Council of Turkey
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7605093/ https://ncbi.nlm.nih.gov/pubmed/32718119 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3906/sag-1901-170 |
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