Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study
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| Description | scientific article |
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author: Filippo Maria Santorelli Matthias R Baumgartner Gioacchino Scarano |
| Publication date | May 1, 2009 |
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