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2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված مقالة علمية (نشرت في سبتمبر 2001) im September 2001 veröffentlichter wissenschaftlicher Artikel artículu científicu espublizáu en 2001 наукова стаття, опублікована у вересні 2001 scientific article (publication date: September 2001) vědecký článek publikovaný v roce 2001 2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած vedecký článok (publikovaný 2001-09) wetenschappelijk artikel (gepubliceerd in 2001-09) ലേഖനം article scientifique publié en 2001
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R K Olsen N Gregersen L Bolund Morten J. Corydon B S Andresen P Bross M J Corydon Niels Gregersen T J Corydon Rikke K.J. Olsen
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Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
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Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
schema:name
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
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10.1002/HUMU.1174 10.1002/HUMU.1174.ABS