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Literature DB >> 17630668

Phenylalanine hydroxylase deficiency exhibits mutation heterogeneity in two large old order Amish settlements.

Abstract

Entities: Disease Gene Mutation

Source DB: PubMed Journal: Am J Med Genet A ISSN： 1552-4825 Impact factor: 2.802

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Authors: Jessica Scott Schwoerer; Nicoletta Drilias; Ashley Kuhl; Sean Mochal; Mei Baker
Journal: Mol Genet Metab Rep Date: 2018-03-08

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