Mutation analysis IVS10-11 G> A in patients with phenylketonuria (PKU) in West Azarbaijan province
عنوان مقاله: Mutation analysis IVS10-11 G> A in patients with phenylketonuria (PKU) in West Azarbaijan province
شناسه ملی مقاله: NCNCMB02_133
منتشر شده در دومین همایش ملی تازه های سلولی و مولکولی در سال 1394
شناسه ملی مقاله: NCNCMB02_133
منتشر شده در دومین همایش ملی تازه های سلولی و مولکولی در سال 1394
مشخصات نویسندگان مقاله:
sasan talaneh - Student Azad University of Ahar Azad
behbod jafari - Assistant Professor Azad University of Ahar
ebrahim mogheisi - Assistant Professor University of Medical Sciences
omid esnaashari - Doctor University of Medical Sciences
خلاصه مقاله:
sasan talaneh - Student Azad University of Ahar Azad
behbod jafari - Assistant Professor Azad University of Ahar
ebrahim mogheisi - Assistant Professor University of Medical Sciences
omid esnaashari - Doctor University of Medical Sciences
PKU is an autosomal recessive disease that converts phenylalanine to tyrosine due to defects in the original .zhn the disease caused by phenylalanine hydroxylase (PAH), which itself is prone to high mutation .jhsh IVS10-11 G> A common Most mutations in the PAH gene and communities in the Mediterranean. Hzf of this study was to determine leap IVS10-11 G> A in patients with PKU in West Azerbaijan province and compare it with many studies in other parts of Iran.
کلمات کلیدی: phenylketonuria, mutation, PAH, PKU
صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/473108/