Low citrulline in Leigh disease: still a biomarker of maternally inherited Leigh syndrome.

Journal of child neurology2010Debray FG, Lambert M, Allard P, et al.

Study designOther primary literature

SubjectHuman

Abstract

cc by 以外（cc by-nc / cc by-nc-nd / NONE 等）は抄録を再掲しない。DOI/PMID へのリンクのみ表示する。

MeSH

AdultArgininosuccinate SynthaseBiomarkersChild, PreschoolCitrullineCitrullinemiaCohort StudiesDNA Mutational AnalysisFemaleGenetic TestingGenotypeHumansInfantLeigh DiseaseMale

DOI 10.1177/0883073809351983

PMID 20472868

View source →