(Q50503087)
Statements
A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation. (English)
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F Kurogouchi
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T Oguchi
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E Mawatari
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S Yamaura
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K Hora
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M Takei
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Y Sekijima
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S i Ikeda
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K Kiyosawa
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1 January 1998
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18
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6
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551-556
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