Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria.-Reference-Cited by-同舟云学术

Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria.

Published:1993-01-09 Issue:6870 Volume:306 Page:115-119
ISSN:0959-8138
Container-title:BMJ
language:en
Short-container-title:BMJ

Author:

Publisher

BMJ

Subject

General Earth and Planetary Sciences,General Environmental Science,General Engineering

Reference41 articles.

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2. The phenylketonuria locus; current knowledge about alleles and mutations of the phenylalanine hydroxvlase gene in various populations;Konecki, D.S.; Lichter-Konecki, U.;Huan Genet,1991

3. The codon 408 mutation associated with haplotye 2 is predominant in Polish families with phenylketonuria;true;Hunt Genet,1991

4. Molecular basis and population genetics of phenylketonuria;Woo, S.L.C.;Biochenntisty,1989

5. Molecular basis of phenotypic heterogeneity in phenylketonuria;Okano, Y.; Eisensmith, R.C.; Guttler, F.; Lichter-Konecki, U.; Konecki, D.S.; Trefz, P.K.;N Engl7Med,1991

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