(Q57263957)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

title

Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1 reference

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

David N. Cooper

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

author name string

C B Grundy

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

M Krawczak

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

J Kobosko

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

V V Kakkar

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

publication date

1 March 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

volume

88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

page(s)

586-588

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00219350

14 September 2019

exact match

0 references

cites work

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

1 reference

https://api.crossref.org/works/10.1007%2FBF00219350

The nucleotide sequence of the gene for human protein C

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219350

MspI RFLP in intron 8 of the human protein C gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219350

Absence of thrombosis in subjects with heterozygous protein C deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219350

Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219350

Hereditary thrombophilia: identification of nonsense and missense mutations in the protein C gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219350

Molecular genetic analysis of a novel form of haemophilia A characterized by the variable expression of factor VIII.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219350

Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1348046

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Application of two neutral MspI DNA polymorphisms in the analysis of hereditary protein C deficiency

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1348046

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The spectrum of genetic defects in a panel of 40 Dutch families with symptomatic protein C deficiency type I: heterogeneity and founder effects

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/1348046

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/BF00219350

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1348046%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1 reference