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Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structure
A loss-of-function mutation in tetratricopeptide repeat domain 7A (TTC7A) is a recently identified cause of human intestinal and immune disorders. However, clues to related underlying molecular dysfunctions remain elusive. It is now shown based on the study of TTC7A-deficient and wild-type cells tha...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232119/ https://www.ncbi.nlm.nih.gov/pubmed/30455981 http://dx.doi.org/10.1038/s41421-018-0061-y |