Creatine deficiency syndrome. a treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiency

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dc.contributor.authorNouioua, S.
dc.contributor.authorCheillan, D.
dc.contributor.authorZaouidi, S.
dc.contributor.authorSalomons, G.S.
dc.contributor.authorAmedjout, N.
dc.contributor.authorKessaci, F.
dc.contributor.authorBoulahdour, N.
dc.contributor.authorHamadouche, T.
dc.contributor.authorTazir, M.
dc.date.accessioned2015-06-04T10:16:27Z
dc.date.available2015-06-04T10:16:27Z
dc.date.issued2013
dc.identifier.issn09608966
dc.identifier.urihttps://dspace.univ-boumerdes.dz123456789/1385
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesVol.23, N°8 (2013);pp. 670–674
dc.subjectCreatine supplementationen_US
dc.subjectL-Arginine:glycine amidinotransferase (GATM)en_US
dc.subjectMyopathyen_US
dc.titleCreatine deficiency syndrome. a treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiencyen_US
dc.typeArticleen_US

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