Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNA <sup>Ser(UCN)</sup> gene
Journal
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- Human Molecular Genetics
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Human Molecular Genetics 4 (8), 1421-1427, 1995
Oxford University Press (OUP)
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Details 詳細情報について
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- CRID
- 1363388844197978368
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- NII Article ID
- 30024453343
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- ISSN
- 14602083
- 09646906
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- Data Source
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- Crossref
- CiNii Articles