Expression Profiling Identifies TWIST2 Target Genes in Setleis Syndrome Patient Fibroblast and Lymphoblast Cells †

Background: Setleis syndrome (SS) is a focal facial dermal dysplasia presenting with bilateral temporal skin lesions, eyelash abnormalities and absent meibomian glands. SS is a rare autosomal recessive disorder caused by mutations in the TWIST2 gene, which codes for a transcription factor of the bHL...

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Detalles Bibliográficos
Autores principales: Crespo, Noe E., Torres-Bracero, Alexandra, Renta, Jessicca Y., Desnick, Robert J., Cadilla, Carmen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922891/
https://www.ncbi.nlm.nih.gov/pubmed/33669496
http://dx.doi.org/10.3390/ijerph18041997

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7922891/
https://www.ncbi.nlm.nih.gov/pubmed/33669496
http://dx.doi.org/10.3390/ijerph18041997

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