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SOXopathies: growing family of developmental disorders due to SOX mutations
The SRY-related (SOX) transcription factor family pivotally contributes to determining cell fate and identity in many lineages. Since the original discovery that SRY deletions cause sex reversal, mutations in half of the twenty human SOX genes have been associated with rare congenital disorders, hen...
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| Publicado en: | Trends Genet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6956857/ https://ncbi.nlm.nih.gov/pubmed/31288943 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tig.2019.06.003 |
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