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3. Phenylalanine hydroxylase deficiency: molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients. Rivera I; Mendes D; Afonso Â; Barroso M; Ramos R; Janeiro P; Oliveira A; Gaspar A; Tavares de Almeida I Mol Genet Metab; 2011; 104 Suppl():S86-92. PubMed ID: 21871829 [TBL] [Abstract][Full Text] [Related]
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5. RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families. Meijer H; Jongbloed RJ; Hekking M; Spaapen LJ; Geraedts JP Hum Genet; 1993 Dec; 92(6):588-92. PubMed ID: 7903270 [TBL] [Abstract][Full Text] [Related]
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9. Mutation screening of phenylketonuria in the Far East of Russia. Sueoka H; Moshinetsky A; Nagao M; Chiba S J Hum Genet; 1999; 44(6):368-71. PubMed ID: 10570906 [TBL] [Abstract][Full Text] [Related]
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12. The molecular basis of phenylalanine hydroxylase deficiency in Croatia. Zschocke J; Preusse A; Sarnavka V; Fumic K; Mardesic D; Hoffmann GF; Baric I Hum Mutat; 2003 Apr; 21(4):399. PubMed ID: 12655552 [TBL] [Abstract][Full Text] [Related]
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20. Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populations. Byck S; Morgan K; Tyfield L; Dworniczak B; Scriver CR Hum Mol Genet; 1994 Sep; 3(9):1675-7. PubMed ID: 7833927 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]