Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patients. | J Hum Genet;44(3): 163-8, 1999. | MEDLINE

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Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patients.

Imamura, T; Okano, Y; Shintaku, H; Hase, Y; Isshiki, G.

Affiliation

Imamura T; Department of Pediatrics, Osaka City University Medical School, Japan.

J Hum Genet ; 44(3): 163-8, 1999.

Article in En | MEDLINE | ID: mdl-10319579

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Phosphorus-Oxygen Lyases / Mutation, Missense / Asian People / Amino Acid Metabolism, Inborn Errors Type of study: Prognostic_studies Limits: Humans / Infant / Male / Newborn Country/Region as subject: Asia Language: En Journal: J Hum Genet Journal subject: GENETICA MEDICA Year: 1999 Document type: Article Affiliation country:

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Collection: 01-internacional Database: MEDLINE Main subject: Phosphorus-Oxygen Lyases / Mutation, Missense / Asian People / Amino Acid Metabolism, Inborn Errors Type of study: Prognostic_studies Limits: Humans / Infant / Male / Newborn Country/Region as subject: Asia Language: En Journal: J Hum Genet Journal subject: GENETICA MEDICA Year: 1999 Document type: Article Affiliation country: