Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations.

Clinical genetics2000da Silva LC, Carvalho TS, da Silva FB, et al.

Study designOther primary literature

SubjectHuman

Abstract

cc by 以外（cc by-nc / cc by-nc-nd / NONE 等）は抄録を再掲しない。DOI/PMID へのリンクのみ表示する。

AspartameDNADNA Mutational AnalysisHeterozygoteHumansMutationPhenylalaninePhenylalanine HydroxylasePhenylketonuriasTyrosine

DOI 10.1034/j.1399-0004.2000.580118.x

PMID 10945671