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Apaf-1 deficiency and neural tube closure defects are found in fog mice
The forebrain overgrowth mutation (fog) was originally described as a spontaneous autosomal recessive mutation mapping to mouse chromosome 10 that produces forebrain defects, facial defects, and spina bifida. Although the fog mutant has been characterized and available to investigators for several y...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC55512/ https://ncbi.nlm.nih.gov/pubmed/11504943 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.171283198 |
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