Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study (Q44268350)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study |
scientific article |
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Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study (English)
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Filippo M Santorelli
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Gioacchino Scarano
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Alessandra Tessa
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Giuseppe Fiermonte
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Carlo Dionisi-Vici
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Eleonora Paradies
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Yin-Hsiu Chien
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Carmela Loguercio
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Helene Ogier de Baulny
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Marie-Cecile Nassogne
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Manuel Schiff
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Federica Deodato
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Giancarlo Parenti
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S Lane Rutledge
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M Antonia Vilaseca
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Mariarosa A B Melone
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Luiz Aldamiz-EchevarrÃa
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Guy Besley
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John Walter
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Eugenia Martinez-Hernandez
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Jose M Hernandez
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Ciro L Pierri
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Ferdinando Palmieri
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1 May 2009
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30
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5
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741-748
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