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Published in 2017 at "Movement Disorders"
DOI: 10.1002/mds.26963
Abstract: Tyrosine hydroxylase deficiency (THD) is a recessive autosomal hereditary disease that blocks the transformation of tyrosine into levodopa, resulting in dystonia and parkinsonism in children (OMIM #605407). Treatment consists of L-dopa, which has variable efficacy.…
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Keywords:
protein redistribution;
tyrosine;
redistribution diet;
tyrosine hydroxylase ... See more keywords