12 results on '"Andreu, A. L."'
Search Results
2. Lack of gastrointestinal symptoms in a 60-year-old patient with MNGIE
3. Phenotypic variability in a Spanish family with MNGIE
4. Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy
5. Molecular genetic analysis of McArdle's disease in Spanish patients
6. Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA
7. Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipation.
8. Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene.
9. Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease.
10. A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2.
11. Reversion of mtDNA depletion in a patient with TK2 deficiency.
12. Analysis of the Cu/Zn Gene in a Catalan ALS Population. Should All Sporadic ALS Cases Also Be Screened for SOD1?
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.