Phenotypic variability among patients with hyperornithinaemia-hyperammonaemiahomocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15

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Veröffentlicht in:	Journal of medical genetics 2008, Vol.45 (11), p.759-764
Hauptverfasser:	DEBRAY, F.-G, LAMBERT, M, LEMIEUX, B, SOUCY, J. F, DROUIN, R, FENYVES, D, DUBE, J, MARANDA, B, LAFRAMBOISE, R, MITCHELL, G. A
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Sprache:	eng
Schlagworte:	Biological and medical sciences Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Medical genetics Medical sciences Molecular and cellular biology
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source	BMJ Journals - NESLi2
subjects	Biological and medical sciences Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Medical genetics Medical sciences Molecular and cellular biology
title	Phenotypic variability among patients with hyperornithinaemia-hyperammonaemiahomocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15
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