المؤلفون: Yutaka Hase, Yasuaki Nishi, Minoru Asada, Yoshiyuki Okano, Youngbo Kang, Toshiaki Oura, Gen Isshiki

المصدر: Human genetics. 103(5)

مصطلحات موضوعية: Phenylalanine hydroxylase, Genotype, Phenylalanine, medicine.disease_cause, Transfection, Hyperphenylalaninemia, Japan, Polymorphism (computer science), Phenylketonurias, Genetics, medicine, Animals, Humans, Genetics (clinical), Mutation, Polymorphism, Genetic, biology, Phenylalanine Hydroxylase, Sequence Analysis, DNA, medicine.disease, Molecular biology, Null allele, Phenotype, COS Cells, biology.protein, Regression Analysis, Restriction fragment length polymorphism, Polymorphism, Restriction Fragment Length

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec34b7f8829750d8ebeb352a9db07601
https://pubmed.ncbi.nlm.nih.gov/9860305