(Q41394453)

30 September 2017

Expression analysis of mutation P244L, which causes mild hyperphenylalaninemia (English)

1 reference

30 September 2017

Pérez B

1

1 reference

30 September 2017

Desviat LR

series ordinal

2

1 reference

30 September 2017

Ugarte M

series ordinal

3

1 reference

30 September 2017

language of work or name

1 reference

1 January 1995

1 reference

30 September 2017

1 reference

30 September 2017

5

1 reference

30 September 2017

2

1 reference

30 September 2017

188-190

1 reference

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

30 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

A new PKU mutation associated with haplotype 12

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Phenylketonuria in Spain: RFLP haplotypes and linked mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Molecular basis of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Localization of cofactor binding sites with monoclonal anti-idiotype antibodies: phenylalanine hydroxylase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locus

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Homology between phenylalanine and tyrosine hydroxylases reveals common structural and functional domains

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Sequence and expression of the Drosophila phenylalanine hydroxylase mRNA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Expression of a preproinsulin-beta-galactosidase gene fusion in mammalian cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Molecular basis of phenotypic heterogeneity in phenylketonuria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Presence of the Mediterranean PKU mutation IVS10 in Latin America

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Genotype-phenotype correlations in phenylketonuria.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380050217

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380050217

1 reference

30 September 2017

1 reference