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Identification of novel mutations in theSLC25A15gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study

Bibliographic reference Tessa, Alessandra ; Fiermonte , Giuseppe ; Dionisi-Vici , Carlo ; Paradies , Eleonora ; Baumgartner m, Matthias R. ; et. al. Identification of novel mutations in theSLC25A15gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: A clinical, molecular, and functional study. In: Human Mutation, Vol. 30, no. 5, p. 741-748 (2009)
Permanent URL http://hdl.handle.net/2078.1/120159
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