(Q50518927)
Statements
Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene. (English)
1 reference
1 reference
F Carella
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A Toscano
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P Soliveri
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P Girlanda
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F Carrara
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G M Fratta
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F M Reid
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C Mariotti
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M Zeviani
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1 August 1995
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4
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8
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1421-1427
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