(Q45890022)

17 December 2017

title

Haemophilia B caused by a point mutation in a donor splice junction of the human factor IX gene (English)

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17 December 2017

main subject

hemophilia

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coagulation factor IX

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1

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17 December 2017

author name string

Rizza CR

series ordinal

2

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17 December 2017

Brownlee GG

series ordinal

3

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17 December 2017

language of work or name

English

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publication date

1 August 1985

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17 December 2017

number of pages

3

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inferred from page(s)

published in

Nature

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17 December 2017

volume

316

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17 December 2017

issue

6029

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17 December 2017

page(s)

643-645

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17 December 2017

https://scigraph.springernature.com/pub.10.1038/316643a0

exact match

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cites work

The gene structure of human anti-haemophilic factor IX.

1 reference

7 January 2021

Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145.

1 reference

7 January 2021

Gene deletions in patients with haemophilia B and anti-factor IX antibodies

1 reference

7 January 2021

The construction of cosmid libraries which can be used to transform eukaryotic cells

1 reference

7 January 2021

Lambdoid phages that simplify the recovery of in vitro recombinants

1 reference

7 January 2021

Colony hybridization: a method for the isolation of cloned DNAs that contain a specific gene

1 reference

7 January 2021

57 Sequencing end-labeled DNA with base-specific chemical cleavages

1 reference

7 January 2021

Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms

1 reference

7 January 2021

Simultaneous rapid chemical synthesis of over one hundred oligonucleotides on a microscale.

1 reference

7 January 2021

Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides

1 reference

7 January 2021

Genetic disorders of human haemoglobin as models for analysing gene regulation

1 reference

7 January 2021

A catalogue of splice junction sequences

1 reference

7 January 2021

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

1 reference

7 January 2021

https://api.fatcat.wiki/v0/release/jrsfeaq6avbo5kwyvvdzloz2oe

Identifiers

1 reference

30 July 2022

mapped directly with Wikidata item

Dimensions Publication ID

1001895769

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Fatcat ID

release_jrsfeaq6avbo5kwyvvdzloz2oe

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jrsfeaq6avbo5kwyvvdzloz2oe

30 July 2022

mapped directly with Wikidata item

1 reference

https://api.fatcat.wiki/v0/release/jrsfeaq6avbo5kwyvvdzloz2oe

30 July 2022