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Acknowledgements Authors are grateful to Panjab University, Chandigarh, India for facilities

Methods 11 , 783784 (2014)

Nutrition & Metabolism, 4 (1), 24

Because the activity of the QDPR gene encoded enzyme is also involved in the functions of the tyrosine hydroxylase and tryptophan hydroxylase enzymes, mutations in the QDPR gene present as atypical hyperphenylalaninemias but are also associated with the potential for microcephaly, hypotonia, intellectual impairment, and convulsions due to neurotransmitter synthesis deficits

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