GLI3 mutations in human disorders mimic Drosophila Cubitus interruptus protein functions and localization
Truncation mutations of the GLI3 zinc finger transcription factor can cause Greig cephalopolysyndactyly syndrome (GCPS), Pallister–Hall syndrome (PHS), and postaxial polydactyly type A (PAP-A). GLI3 is homologous to Drosophila Cubitus interruptus (Ci), which regulates the patched (ptc), gooseberry (...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1999
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC15863/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10077605/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.6.2880 |
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