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Fecha Publicación: 2005-12-23
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Osorio O., J. H. (2005). Errores innatos del metabolismo, un grupo importante de enfermedades raras. Biosalud, 4, -. Recuperado a partir de https://revistasojs.ucaldas.edu.co/index.php/biosalud/article/view/5855
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Garrod A.E. The incidente of alkaptonuria: a study in clinical individuality. Lancet, 1902. 2:1616-1620.
Garrod A.E. The Croonian Lectures on inborn errors of metabolism. Lecture II. Alcaptonuria. Lancet, 1908. 2:73-79.
LaDu B.N., Zannoni V.A., Laster L., Seegmiller J.E., The nature of the defect in tyrosine metabolism in alcaptonuria. J. Biol. Chem, 1958. 230:251.
Mullis K., Faloona F., Scharf S., Saiki R., Horn G., Erlich H. Enzymatic amplification of DNA in vitro: The polymerase chain reaction. Cold Spring Harb. Symp. Quant. Biol, 1986.11:1-3.
Osorio J.H., García F., Sánchez A. First report for 625G>A polymorphism in the shortchain acyl-CoA dehydrogenase in South América. J. Inherit. Metab. Dis, 2005. 28:109.
Garrod A.E. The Croonian Lectures on inborn errors of metabolism. Lecture II. Alcaptonuria. Lancet, 1908. 2:73-79.
LaDu B.N., Zannoni V.A., Laster L., Seegmiller J.E., The nature of the defect in tyrosine metabolism in alcaptonuria. J. Biol. Chem, 1958. 230:251.
Mullis K., Faloona F., Scharf S., Saiki R., Horn G., Erlich H. Enzymatic amplification of DNA in vitro: The polymerase chain reaction. Cold Spring Harb. Symp. Quant. Biol, 1986.11:1-3.
Osorio J.H., García F., Sánchez A. First report for 625G>A polymorphism in the shortchain acyl-CoA dehydrogenase in South América. J. Inherit. Metab. Dis, 2005. 28:109.
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