neonatal screening for phenylketonuria

Faculty	Medicine	Year:	1993
Type of Publication:	Theses	Pages:	138
Authors:	Ahlam Ahmed Mohamed Ahmed
		BibID	11052495
Keywords :	pediatrics
Abstract:	phenylketonuria is an autosomal recessive disorder of phenylalanine metabolism caused by decreased activity of phenylalanine hydroxylase enzyme wich is responsible for conversion of phenylalanine to tyrosine.

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