(Q59689181)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1358783%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

title

CpG hotspot causes second mutation in codon 408 of the phenylalanine hydroxylase gene (English)

1 reference

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14 September 2019

1

1 reference

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14 September 2019

author name string

S M Forrest

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1358783%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

J A Saleeba

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1358783%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

R G Cotton

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1358783%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

publication date

1 September 1992

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14 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1358783%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

volume

90

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14 September 2019

issue

1-2

1 reference

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14 September 2019

page(s)

147-148

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https://scigraph.springernature.com/pub.10.1007/bf00210760

14 September 2019

exact match

0 references

cites work

Missense mutations prevalent in Orientals with phenylketonuria: molecular characterization and clinical implications

1 reference

12 December 2020

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

12 December 2020

Phenylketonuria and other phenylalanine hydroxylation mutants in man.

1 reference

12 December 2020

Molecular basis of base substitution hotspots in Escherichia coli

1 reference

12 December 2020

Improvement of PCR amplified DNA sequencing with the aid of detergents

1 reference

12 December 2020

Missense mutations associated with RFLP haplotypes 1 and 4 of the human phenylalanine hydroxylase gene.

1 reference

12 December 2020

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria

1 reference

12 December 2020

Screening for phenylketonuria mutations by DNA amplification with the polymerase chain reaction

1 reference

12 December 2020

An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.

1 reference

12 December 2020

CpG dinucleotides are mutation hot spots in phenylketonuria

1 reference

12 December 2020

The CpG dinucleotide and human genetic disease

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00210760

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1358783%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1 reference