Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15
Debray, F-G, Lambert, M, Lemieux, B, Soucy, J F, Drouin, R, Fenyves, D, Dube, J, Maranda, B, Laframboise, R, Mitchell, G AТом:
45
Мова:
english
Журнал:
Journal of Medical Genetics
DOI:
10.1136/jmg.2008.059097
Date:
November, 2008
Файл:
PDF, 272 KB
english, 2008
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