Nuclear suppression of a mitochondrial RNA splice defect: nucleotide sequence and disruption of the MRS3 gene
✍ Scribed by Schmidt, Cornelia ;Söllner, Thomas ;Schweyen, Rudolf J.
- Publisher
- Springer
- Year
- 1987
- Tongue
- English
- Weight
- 800 KB
- Volume
- 210
- Category
- Article
- ISSN
- 0026-8925
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The plant mitochondrial genome encodes several subunits of the ATP synthase (ATPase) complex including the alpha subunit of the catalytic F~portion (atpA) and subunits 6 and 9 of the proton-translocating Fo-portion (atp6 and atp9 ). In
Autosomal dominant polycystic kidney disease (ADPKD) occurs mainly from mutations of polycystic kidney disease 1 (PKD1) gene. A novel mutation of the PKD1 gene due to a nucleotide substitution in splice-acceptor site of IVS13 (AG->TG) was identified by analyses of PKD1-cDNA and genomic DNA. The IVS1