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Genetic history of phenylketonuria mutations in Italy.
Dianzani I, Giannattasio S, de Sanctis L, Marra E, Ponzone A, Camaschella C, Piazza A. Dianzani I, et al. Am J Hum Genet. 1994 Oct;55(4):851-3. Am J Hum Genet. 1994. PMID: 7942862 Free PMC article. No abstract available.
Characterization of phenylketonuria alleles in the Italian population.
Dianzani I, Giannattasio S, de Sanctis L, Alliaudi C, Lattanzio P, Dionisi Vici C, Burlina A, Burroni M, Sebastio G, Carnevale F, et al. Dianzani I, et al. Eur J Hum Genet. 1995;3(5):294-302. doi: 10.1159/000472313. Eur J Hum Genet. 1995. PMID: 8556304
A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype.
Guldberg P, Rey F, Zschocke J, Romano V, François B, Michiels L, Ullrich K, Hoffmann GF, Burgard P, Schmidt H, Meli C, Riva E, Dianzani I, Ponzone A, Rey J, Güttler F. Guldberg P, et al. Among authors: dianzani i. Am J Hum Genet. 1998 Jul;63(1):71-9. doi: 10.1086/301920. Am J Hum Genet. 1998. PMID: 9634518 Free PMC article.
157 results