(Q45862874)

17 December 2017

title

Origin of mutation in sporadic cases of haemophilia A. (English)

1 reference

17 December 2017

0 references

0 references

Ljung RC

1

1 reference

17 December 2017

Sjörin E

series ordinal

2

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17 December 2017

language of work or name

English

0 references

publication date

1 September 1999

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17 December 2017

British Journal of Haematology

published in

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17 December 2017

volume

106

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17 December 2017

issue

4

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17 December 2017

page(s)

870-874

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17 December 2017

Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1999.01631.X

Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1999.01631.X

Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1999.01631.X

The haemophilia A mutation search test and resource site, home page of the factor VIII mutation database: HAMSTeRS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1999.01631.X

Characterization of genetic defects of hemophilia A in patients of Chinese origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1999.01631.X

10.1046/J.1365-2141.1999.01631.X

21 January 2018

Identifiers

DOI

1 reference

17 December 2017

release_2uk6hbmcendpdcai4bfpa5ywue

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2uk6hbmcendpdcai4bfpa5ywue

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

10519986

1 reference

17 December 2017