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A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling
Meckel syndrome (MKS) is a rare autosomal recessive disease causing perinatal lethality associated with a complex syndrome that includes occipital meningoencephalocele, hepatic biliary ductal plate malformation, postaxial polydactyly and polycystic kidneys. The gene mutated in type 1 MKS encodes a p...
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| Autores principales: | , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Oxford University Press
2009
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2773271/ https://ncbi.nlm.nih.gov/pubmed/19776033 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp422 |
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