A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy
SMN1 and SMN2 (survival motor neuron) encode identical proteins. A critical question is why only the homozygous loss of SMN1, and not SMN2, results in spinal muscular atrophy (SMA). Analysis of transcripts from SMN1/SMN2 hybrid genes and a new SMN1 mutation showed a direct relationship between prese...
Guardado en:
| Publicado en: | Proc Natl Acad Sci U S A |
|---|---|
| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
National Academy of Sciences
1999
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC26877/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10339583/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.11.6307 |
| Etiquetas: |
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
