Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria

Background: Phenylketonuria as the most common genetic metabolic disorder is the result of disruption of the phenylalanine hydroxylase gene. This study was carried out to explore the phenylalanine hydroxylase gene mutation status of Iranian phenylketonuria patients. Methods: Blood samples were colle...

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Detalles Bibliográficos
Autores principales: Rastegar Moghadam, Mahsa, Shojaei, Azadeh, Babaei, Vahid, Rohani, Farzaneh, Ghazi, Farideh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iran University of Medical Sciences 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108261/
https://www.ncbi.nlm.nih.gov/pubmed/30159272
http://dx.doi.org/10.14196/mjiri.32.21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108261/
https://www.ncbi.nlm.nih.gov/pubmed/30159272
http://dx.doi.org/10.14196/mjiri.32.21

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