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dc.contributor.authorKaufman, Mimi
dc.contributor.authorNardella, Maria
dc.date.accessioned2014-08-01T21:54:32Z
dc.date.available2014-08-01T21:54:32Z
dc.date.issued1985
dc.identifier.urihttp://repositorio.ub.edu.ar/handle/123456789/2808
dc.description.abstractPhenylketonuria (or PKU) is an inherited disorder of protein metabolism. Children with PKU do not have a functioning enzyme to metabolize or break down amino acid call phenylalanine (PHE for short), which is found in all food proteins. Protein in foods is important for building and repairing the body's tissues. Amino acids are often called the "building blocks" of protein. Twenty-two amino acids can be joined together in various combinations to form all the different kinds of proteins in foods. Enzymes are special substances in the body which work to separate the amino acids in food proteins and recombine them to form the different proteins which the body needs.es_ES
dc.language.isoenes_ES
dc.publisher.EditorUniversidad de Belgrano - Documentos CEEGMD - Centro para el estudio de enfermedades genéticas, metabólicas y discapacidades. Facultad de Ciencias Exactas
dc.relation.ispartofseriesDocumentos CEEGMD;July 1985
dc.subjectTeacheres_ES
dc.subjectPKUes_ES
dc.subjectmaestroes_ES
dc.subjectPhenylketonuriaes_ES
dc.subjectfenilcetonuriaes_ES
dc.subjectprotein metabolismes_ES
dc.subjectmetabolismo de las proteínases_ES
dc.titleA Teacher's Guide to PKUes_ES
dc.typeLearning Objectes_ES


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