Decrease of 3243 A→G mtDNA Mutation from Blood in MELAS Syndrome: A Longitudinal Study-Reference-Cited by-同舟云学术

Decrease of 3243 A→G mtDNA Mutation from Blood in MELAS Syndrome: A Longitudinal Study

Published:2001-01 Issue:1 Volume:68 Page:238-240
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Rahman S.,Poulton J.,Marchington D.,Suomalainen A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference18 articles.

1. MELAS: clinical features, biochemistry, and molecular genetics;Ciafaloni;Ann Neurol,1992

2. Longitudinal study of a heteroplasmic 3460 Leber hereditary optic neuropathy family by multiplexed primer-extension analysis and nucleotide sequencing;Ghosh;Am J Hum Genet,1996

3. A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies;Goto;Nature,1990

4. Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples;Hammans;Lancet,1991

5. A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes);Kobayashi;Biochem Biophys Res Commun,1990

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