Nalaganje...
The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
OBJECTIVE--To verify the phenotype to genotype correlations of mitochondrial DNA (mtDNA) related disorders in an atypical maternally inherited encephalomyopathy. METHODS--Neuroradiological, morphological, biochemical, and molecular genetic analyses were performed on the affected members of a pedigre...
Shranjeno v:
| izdano v: | J Neurol Neurosurg Psychiatry |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BMJ Publishing Group
1996
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC486456/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8676159/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jnnp.61.1.47 |
| Oznake: |
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