Zobrazeno 1 - 1
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pro vyhledávání: '"Maitha Almakhari"'
Autor:
Maitha Almakhari, Yan Chen, Amanda Shen-Yee Kong, Danesh Moradigaravand, Kok-Song Lai, Swee-Hua Erin Lim, Jiun-Yan Loh, Sathiya Maran
Publikováno v:
PLoS ONE, Vol 19, Iss 6, p e0298092 (2024)
The TBX1 gene plays a critical role in the development of 22q11.2 deletion syndrome (22q11.2DS), a complex genetic disorder associated with various phenotypic manifestations. In this study, we performed in-silico analysis to identify potentially dele
Externí odkaz:
https://doaj.org/article/01516a3f0dd94618a2a00a40cde675d6
