Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland
about
Phenylketonuria: translating research into novel therapiesA system for specific, high-throughput genotyping by allele-specific primer extension on microarrays.Current situation and prospects of newborn screening and treatment for Phenylketonuria in China - compared with the current situation in the United States, UK and Japan.Phenylketonuria: an inborn error of phenylalanine metabolism.Sequence variation at the phenylalanine hydroxylase gene in the British Isles.Antioxidant treatment strategies for hyperphenylalaninemia.Mechanisms of Inflammation-Associated Depression: Immune Influences on Tryptophan and Phenylalanine Metabolisms.The status of neonatal screening in China, 2013.Phenylketonuria: A new look at an old topic, advances in laboratory diagnosis, and therapeutic strategies.Hyperphenylalaninaemias in Estonia: Genotype-Phenotype Correlation and Comparative Overview of the Patient Cohort Before and After Nation-Wide Neonatal Screening.Diagnostic and therapeutic recommendations for the treatment of hyperphenylalaninemia in patients 0-4 years of age
P2860
Q27015749-CDD7EBCF-3E18-4D1B-AA7B-0A8A26078D0AQ30651566-8C00BC71-9EF9-471B-99E1-D9E8557840A6Q34377810-757419FD-8BCB-491E-AD59-32B1DBAC022DQ34787712-0CC14C87-AA41-4FB5-B133-A7EB5539EF44Q35238355-6868A48E-3988-43EC-A042-B5BF832165DDQ38105266-321C9DC2-A87D-4768-A7B7-407B12A59052Q38859547-04C303A3-0D31-475D-B218-7B6FE0D2637FQ40665128-0FD742B1-1493-44FE-9A32-42C43C5D8BF4Q45874121-C6F389FF-6943-431A-A4F4-13BA720C151FQ47909624-F9DF58D4-61A9-42ED-8CDB-D3A61D9E8DAFQ58795807-ABD0423A-4D92-4BD6-A86B-6252C459A95E
P2860
Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland
description
1995 nî lūn-bûn
@nan
1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Phenylketonuria in a low incid ...... sation of mutations in Finland
@ast
Phenylketonuria in a low incid ...... sation of mutations in Finland
@en
Phenylketonuria in a low incid ...... sation of mutations in Finland
@en-gb
Phenylketonuria in a low incid ...... sation of mutations in Finland
@nl
type
label
Phenylketonuria in a low incid ...... sation of mutations in Finland
@ast
Phenylketonuria in a low incid ...... sation of mutations in Finland
@en
Phenylketonuria in a low incid ...... sation of mutations in Finland
@en-gb
Phenylketonuria in a low incid ...... sation of mutations in Finland
@nl
prefLabel
Phenylketonuria in a low incid ...... sation of mutations in Finland
@ast
Phenylketonuria in a low incid ...... sation of mutations in Finland
@en
Phenylketonuria in a low incid ...... sation of mutations in Finland
@en-gb
Phenylketonuria in a low incid ...... sation of mutations in Finland
@nl
P2093
P2860
P356
P1476
Phenylketonuria in a low incid ...... sation of mutations in Finland
@en
P2093
A de la Chapelle
K F Henriksen
P Guldberg
P2860
P356
10.1136/JMG.32.12.976
P407
P577
1995-12-01T00:00:00Z