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Genetic mutation of Frem3 does not cause Fraser syndrome in mice
QBRICK, FRAS1, and FREM2 compose a family of extracellular matrix proteins characterized by twelve consecutive CSPG repeats and single or multiple Calx-β motifs. Dysfunction of these proteins have been associated with Fraser syndrome, which is characterized by malformation of skin, eyes, digits, and...
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| Publicado no: | Exp Anim |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Japanese Association for Laboratory Animal Science
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7004800/ https://ncbi.nlm.nih.gov/pubmed/31554749 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1538/expanim.19-0088 |
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