A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) - Concepedia

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A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)

371

Citations

25

References

1990

Year

Yoko Kobayashi, Mariko Y. Momoi, Kaoru Tominaga, Takashi Momoi, Kenji Nihei, Masayoshi Yanagisawa, Yasuo Kagawa, Shigeo Ohta

Biochemical and Biophysical Research Communications

Mitochondrial MyopathyMitochondrial FunctionGenetic DisorderGeneticsPathologyPoint MutationMitochondrial MedicineMolecular GeneticsDisease Gene IdentificationGenomicsMitochondrial TrnaleuMedicine

References

	Year	Citations

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