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Genetic mutations in ribosomal biogenesis gene TCOF1 identified in human neural tube defects.

Fang WangHaiqin ChengQin ZhangJin Guo
Published in: Molecular genetics & genomic medicine (2023)
This study explored the functional impact of a missense variant in TCOF1, implicating a set of novel causative biological factors involved in the pathogenicity of human NTDs, particularly whom combined with craniofacial abnormality.
Keyphrases
  • endothelial cells
  • induced pluripotent stem cells
  • genome wide
  • pluripotent stem cells
  • copy number
  • intellectual disability
  • gene expression
  • dna methylation
  • staphylococcus aureus
  • pseudomonas aeruginosa