Variations in genotype-phenotype correlations in phenylketonuria patients.
about
Phenylalanine hydroxylase deficiency.Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates population.Molecular characterisation of phenylketonuria in a Chinese mainland population using next-generation sequencing.Systematic Review and Meta-Analysis of Neuropsychiatric Symptoms and Executive Functioning in Adults With Phenylketonuria.Molecular epidemiology, genotype-phenotype correlation and BH4 responsiveness in Spanish patients with phenylketonuria.Estimating the allele frequency of autosomal recessive disorders through mutational records and consanguinity: the Homozygosity Index (HI).Mutations of the phenylalanine hydroxylase gene in Iranian patients with phenylketonuriaMutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations.
P2860
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P2860
Variations in genotype-phenotype correlations in phenylketonuria patients.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Variations in genotype-phenotype correlations in phenylketonuria patients.
@en
Variations in genotype-phenotype correlations in phenylketonuria patients.
@nl
type
label
Variations in genotype-phenotype correlations in phenylketonuria patients.
@en
Variations in genotype-phenotype correlations in phenylketonuria patients.
@nl
altLabel
Variations in genotype-phenotype correlations in phenylketonuria patients
@en
prefLabel
Variations in genotype-phenotype correlations in phenylketonuria patients.
@en
Variations in genotype-phenotype correlations in phenylketonuria patients.
@nl
P2093
P356
P1476
Variations in genotype-phenotype correlations in phenylketonuria patients
@en
P2093
A L P Starling
C G Fonseca
J N Januário
M G C D Peixoto
M J B Aguiar
P356
10.4238/VOL9-1GMR670
P577
2010-01-05T00:00:00Z