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Novel IRF6 mutations in Chinese Han families with Van der Woude syndrome
BACKGROUND: Interferon Regulatory Factor 6 (IRF6) gene encodes a member of the IRF family of transcription factors. Mutations in IRF6 cause Van der Woude Syndrome (VWS), which is the most common malformation of syndromic orofacial clefts in humans. METHODS: Here, we performed sequencing studies of s...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7216816/ https://ncbi.nlm.nih.gov/pubmed/32108996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1196 |
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