(Q45213018)

English

Homozygous nonsense mutation (Cys72-->stop) in the human F7 gene: a not life-threatening mutation despite the absence of circulating factor VII.

scientific article published in January 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

Homozygous nonsense mutation (Cys72-->stop) in the human F7 gene: a not life-threatening mutation despite the absence of circulating factor VII. (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

1 reference

based on heuristic

inferred from title

author name string

Chafa O

1

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

Fischer AM

2

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

Reghis A

3

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

Tapon-Bretaudiere J

4

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

Journal of Thrombosis and Haemostasis

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

175-177

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2004.01089.X

21 January 2018

Factor VII deficiency and the FVII mutation database

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2004.01089.X

21 January 2018

Factor VII Deficiency

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2004.01089.X

21 January 2018

Two novel cases of cerebral haemorrhages at the neonatal period associated with inherited factor VII deficiency, one of them revealing a new nonsense mutation (Ser52Stop).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2004.01089.X

21 January 2018

Factor VII gene intronic mutation in a lethal factor VII deficiency: effects on splice-site selection.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2004.01089.X

21 January 2018

Mice lacking factor VII develop normally but suffer fatal perinatal bleeding

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2004.01089.X

21 January 2018

Prenatal exclusion of severe factor VII deficiency by DNA sequencing

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2004.01089.X

21 January 2018

Identifiers

10.1111/J.1538-7836.2004.01089.X

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 December 2017

ResearchGate publication ID

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