(Q44492256)

English

A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosis

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

0 references

David N. Cooper

5

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

author name string

C B Grundy

1

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

S Holding

2

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

D S Millar

3

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

V V Kakkar

4

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

publication date

1 March 1992

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

88

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

707-708

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

The use of an automated analyzer in the evaluation of antithrombin III and heparin

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular genetics of familial venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial antithrombin III deficiency: its natural history, genetics, diagnosis and treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent deletion in the human antithrombin III gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of the human antithrombin III structural gene to chromosome 1q23-25

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antithrombin III Utah: proline-407 to leucine mutation in a highly conserved region near the inhibitor reactive site

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

cDNA cloning and expression in Escherichia coli of a plasminogen activator inhibitor from human placenta

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intron structure of the human antithrombin III gene differs from that of other members of the serine protease inhibitor superfamily

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antithrombin III deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1551681

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF02265306

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q44492256&oldid=2206685673"