(Q43526802)
Statements
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Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome (English)
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Tsujino S
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Kanazawa N
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Ohashi T
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Eto Y
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Saito T
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Kira J
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Yamada T
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1 May 2000
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47
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5
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625-631
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Identifiers
1 reference
1 reference