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Biochemical defects in minor spliceosome function in the developmental disorder MOPD I
Biallelic mutations of the human RNU4ATAC gene, which codes for the minor spliceosomal U4atac snRNA, cause the developmental disorder, MOPD I/TALS. To date, nine separate mutations in RNU4ATAC have been identified in MOPD I patients. Evidence suggests that all of these mutations lead to abrogation o...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Cold Spring Harbor Laboratory Press
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4114687/ https://ncbi.nlm.nih.gov/pubmed/24865609 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1261/rna.045187.114 |
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