Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in Thailand

© 2017 The Author(s). Background: Hyperphenylalaninemia (HPA) can be classified into phenylketonuria (PKU) which is caused by mutations in the phenylalanine hydroxylase (PAH) gene, and BH4 deficiency caused by alterations in genes involved in tetrahydrobiopterin (BH4) biosynthesis pathway. Dietary r...

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Bibliographic Details
Main Authors: Chaiyasap P., Ittiwut C., Srichomthong C., Sangsin A., Suphapeetiporn K., Shotelersuk V.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85029433997&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40107
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Institution: Chiang Mai University