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Syndromic immune disorder caused by a viable hypomorphic allele of spliceosome component Snrnp40
We report a new immunodeficiency disorder in mice caused by a viable hypomorphic mutation of Snrnp40, an essential gene encoding a subunit of the U5 small nuclear ribonucleoprotein (snRNP) complex of the spliceosome. Snrnp40 is ubiquitous but strongly expressed in lymphoid tissue. Homozygous mutant...
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| Publicado en: | Nat Immunol |
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| Autores principales: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7179765/ https://ncbi.nlm.nih.gov/pubmed/31427773 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41590-019-0464-4 |
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