Transient neonatal hyperphenylalaninaemia is not related to mutations at the phenylalanine hydroxylase gene.

doi:10.1007/BF00710439

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Article

Transient neonatal hyperphenylalaninaemia is not related to mutations at the phenylalanine hydroxylase gene.

Journal of inherited metabolic disease - 1 Jan 1995

Zschocke J, Carson D J

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Share to Amino Acid Metabolism, Inborn Errors
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 7474914
DOI: 10.1007/BF00710439

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Transient neonatal hyperphenylalaninaemia is not related to mutations at the phenylalanine hydroxylase gene.PMID 7474914Read ↗

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Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria.Semantic proximity Read ↗

Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype.Semantic proximity Read ↗

[What should the paediatrician know about hyperphenylalaninaemia?].Semantic proximity Read ↗

R252W/E178G phenylalanine hydroxylase genotype in a Romanian non-PKU hyperphenylalaninaemic patient.Semantic proximity Read ↗

Molecular basis for the phenotypical diversity of phenylketonuria and related hyperphenylalaninaemias.Semantic proximity Read ↗

"Mild" hyperphenylalaninemia? A case series of seven treated patients following newborn screening.Semantic proximity Read ↗

Neonatal phenylalanine wash-out in phenylketonuria.Semantic proximity Read ↗

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