Novel homozygous mutation of phenylalanine hydroxylase gene in a Chinese patient with phenylketonuria

Open Access

1 June 1993

journal article
research article
Published by Oxford University Press (OUP) in Clinical Chemistry

Vol. 39 (6) , 1350
https://doi.org/10.1093/clinchem/39.6.1350

Abstract

Y Takarada, K Yamashita, N Ohtsuka, S Kagawa, A Matsuoka; Novel homozygous mutation of phenylalanine hydroxylase gene in a Chinese patient with phenylketonuria

Keywords

HOMOZYGOUS MUTATION
PHENYLALANINE HYDROXYLASE GENE
MUTATION OF PHENYLALANINE
NOVEL HOMOZYGOUS
PATIENT WITH PHENYLKETONURIA