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savio-l-c documents
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α1-Antitrypsin deficiency detection by direct analysis of the mutation in the gene
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Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria
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An ammo-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2
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Molecular basis and population genetics of phenylketonuria
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Hepatic Gene Therapy: Persistent Expression of Human α1-Antitrypsin in Mice after Direct Gene Delivery In Vivo
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Molecular evolution of serpins: homologous structure of the human .alpha.1-antichymotrypsin and .alpha.1-antitrypsin genes
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5' Domain and nucleotide sequence of an adult chicken chromosomal .beta.-globin gene
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Homology between phenylalanine and tyrosine hydroxylases reveals common structural and functional domains
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Structural characterization of the 5' regions of the human phenylalanine hydroxylase gene
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Phenylalanine hydroxylase deficiency caused by a single base substitution in an exon of the human phenylalanine hydroxylase gene
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Molecular evolution of serpins: homologous structure of the human .alpha.1-antichymotrypsin and .alpha.1-antitrypsin genes [Erratum to document cited in CA107(25):230423x]
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Assessment of Recombinant Adenoviral Vectors for Hepatic Gene Therapy
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Evaluation of Relative Promoter Strength in Primary Hepatocytes Using Optimized Lipofection
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A Simple and Efficient Method for the Concentration and Purification of Recombinant Retrovirus for Increased Hepatocyte Transduction In Vivo