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Lack of TCF2/vHNF1 in mice leads to pancreas agenesis
Heterozygous mutations in the human POU-homeobox TCF2 (vHNF1, HNF1β) gene are associated with maturity-onset diabetes of the young, type 5, and abnormal urogenital tract development. Recently, pancreas atrophies have been reported in several maturity-onset diabetes of the young type 5 patients, sugg...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC547822/ https://ncbi.nlm.nih.gov/pubmed/15668393 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0405776102 |
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