Molecular characterization of phenylketonuria in Japanese patients.

Okano, Y; Asada, M; Kang, Y; Nishi, Y; Hase, Y; Oura, T; Isshiki, G

Okano, Y; Asada, M; Kang, Y; Nishi, Y; Hase, Y; Oura, T; Isshiki, G.

Affiliation

Okano Y; Department of Pediatrics, Osaka City University Medical School, Japan. okano@med.osaka-cu.ac.jp

Hum Genet ; 103(5): 613-8, 1998 Nov.

Article in En | MEDLINE | ID: mdl-9860305

Subject(s)

Phenylalanine Hydroxylase/genetics; Phenylketonurias/genetics; Animals; COS Cells; Genotype; Humans; Japan; Mutation/genetics; Phenotype; Phenylalanine/blood; Polymorphism, Genetic/genetics; Polymorphism, Restriction Fragment Length; Regression Analysis; Sequence Analysis, DNA; Transfection/genetics

Search on Google

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Phenylalanine Hydroxylase / Phenylketonurias Type of study: Diagnostic_studies Limits: Animals / Humans Country/Region as subject: Asia Language: En Journal: Hum Genet Year: 1998 Document type: Article

Search on Google

XML

PubMed Links