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Mechanistic studies in Drosophila and chicken give new insights into functions of DVL1 in dominant Robinow syndrome
The study of rare genetic diseases provides valuable insights into human gene function. The autosomal dominant or autosomal recessive forms of Robinow syndrome are genetically heterogeneous, and the common theme is that all the mutations lie in genes in Wnt signaling pathways. Cases diagnosed with R...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Company of Biologists Ltd
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120075/ https://www.ncbi.nlm.nih.gov/pubmed/36916233 http://dx.doi.org/10.1242/dmm.049844 |