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tieteellinen artikkeli επιστημονικό άρθρο 2003年學術文章 vetenskaplig artikel научна статия scientific article published in January 2003 บทความทางวิทยาศาสตร์ articol științific научни чланак 2003年学术文章 научни чланак vedecký článok artigo científico vitskapeleg artikkel naučni članak 2003年学术文章 artículu científicu 2003年學術文章 bilimsel makale artikull shkencor scientific article published in January 2003 наукова стаття, опублікована в січні 2003 2003년 논문 2003 nî lūn-bûn wissenschaftlicher Artikel мақолаи илмӣ 2003年學術文章 জানুয়ারি ২০০৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ научная статья artykuł naukowy vitenskapelig artikkel article científic სამეცნიერო სტატია 2003年学术文章 2003年学术文章 artigo científico bài báo khoa học 2003年学术文章 artículo científico publicado en 2003 2003年の論文 2003年學術文章 مقالة علمية نشرت في يناير 2003 artikulong pang-agham scienca artikolo scientific article published in January 2003 artikel ilmiah videnskabelig artikel 2003年學術文章 article scientific wetenschappelijk artikel articolo scientifico article scientifique teaduslik artikkel artigo científico מאמר מדעי 2003年学术文章 tudományos cikk vědecký článek

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E P Treacy A Lee-Chong S Ryan G Roche S Goodman B Lynch

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Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype. Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.

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Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype. Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.

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Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype. Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.

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Profound neurological presentation resulting from homozygosity for a mild glutaryl-CoA dehydrogenase mutation with a minimal biochemical phenotype.

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