COMPARATIVE STUDY BETWEEN THE PHENYLALANINE LEVEL IN UMBILICAL CORD BLOOD AND IN HEEL PRICK BLOOD OF THE NEWBORN
Omayma Abd El Kader Hashem Morsy;
Abstract
ABSTRACT
Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine (Phe) metabolism resulting from deficiency of phenylalanine hydroxylase (PAH). Most forms of PKU and hyperphenylalaninaemia (HPA) are caused by mutations in the PAH g
Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine (Phe) metabolism resulting from deficiency of phenylalanine hydroxylase (PAH). Most forms of PKU and hyperphenylalaninaemia (HPA) are caused by mutations in the PAH g
Other data
| Title | COMPARATIVE STUDY BETWEEN THE PHENYLALANINE LEVEL IN UMBILICAL CORD BLOOD AND IN HEEL PRICK BLOOD OF THE NEWBORN | Other Titles | دراسة مقارنة بيـن مستوي الفينيل ألانيـن في دم الحبل السري و في دم وخزة الكعب لحديثي الولادة | Authors | Omayma Abd El Kader Hashem Morsy | Keywords | COMPARATIVE STUDY BETWEEN THE PHENYLALANINE LEVEL IN UMBILICAL CORD BLOOD AND IN HEEL PRICK BLOOD OF THE NEWBORN | Issue Date | 2012 | Description | ABSTRACT Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine (Phe) metabolism resulting from deficiency of phenylalanine hydroxylase (PAH). Most forms of PKU and hyperphenylalaninaemia (HPA) are caused by mutations in the PAH g |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| All Thesis.pdf | 147.66 kB | Adobe PDF | View/Open |
Similar Items from Core Recommender Database
Items in Ain Shams Scholar are protected by copyright, with all rights reserved, unless otherwise indicated.