Zobrazeno 1 - 1
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pro vyhledávání: '"Dávid Vrábel"'
Autor:
Monika Nováková, Marek Hampl, Dávid Vrábel, Jan Procházka, Silvia Petrezselyová, Michaela Procházková, Radislav Sedláček, Michaela Kavková, Tomáš Zikmund, Jozef Kaiser, Hsien-Chia Juan, Ming-Ji Fann, Marcela Buchtová, Jiří Kohoutek
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Congenital heart defects, dysmorphic facial features and intellectual developmental disorders (CHDFIDD) syndrome in humans was recently associated with mutation in CDK13 gene. In order to assess the loss of function of Cdk13 during mouse development,
Externí odkaz:
https://doaj.org/article/4d41af9129ff4519a62d72b8f5b0b1e8
