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The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis
Fraser syndrome is a rare recessive disorder characterized by cryptophthalmos, syndactyly, renal defects, and a range of other developmental abnormalities. Because of their extensive phenotypic overlap, the mouse blebbing mutants have been considered models of this disorder, and the recent isolation...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC518794/ https://ncbi.nlm.nih.gov/pubmed/15345741 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0402760101 |
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