Hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome with evidence of mitochondrial dysfunction due to a novel SLC25A15 (ORNT1) gene mutation in a Palestinian family

Author: Korman S.H.   Kanazawa N.   Abu-Libdeh B.   Gutman A.   Tsujino S.  

Publisher: Elsevier

ISSN: 0022-510X

Source: Journal of the Neurological Sciences, Vol.218, Iss.1, 2004-03, pp. : 53-58

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