Two unusual clinical presentations of the mitochondrial DNA A3243G point mutation in adult neurological practice.
Open Access
- 1 May 1997
- journal article
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 62 (5), 544-546
- https://doi.org/10.1136/jnnp.62.5.544
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- The mitochondrial DNA transfer RNA Leu(UUR) A→G(3243) mutation: A clinical and genetic studyBrain, 1995
- Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patientsBrain, 1995
- Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNANeuromuscular Disorders, 1993
- MELAS: Clinical features, biochemistry, and molecular geneticsAnnals of Neurology, 1992
- MELAS: An original case and clinical criteria for diagnosisNeuromuscular Disorders, 1992
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Mitochondrial diseasesTrends in Neurosciences, 1986