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المؤلفون: R. Zufferey, Dominique Belin, Béatrice Conne
المصدر: Journal of Inherited Metabolic Disease, Vol. 18, No 5 (1995) pp. 577-583
مصطلحات موضوعية: Male, Population, Molecular Sequence Data, Physiology, Biology, ddc:616.07, Heterozygote Detection, Asymptomatic, Acyl-CoA Dehydrogenase, Medium-chain acyl-CoA dehydrogenase, Acyl-CoA Dehydrogenases, Genetics, medicine, Humans, education, Gene, Genetics (clinical), education.field_of_study, Base Sequence, Acyl-CoA Dehydrogenases/ genetics, Genetic Carrier Screening, Acyl CoA dehydrogenase, Mutation (genetic algorithm), Cohort, Mutation, Etiology, biology.protein, Female, medicine.symptom, Switzerland