(Q33835317)

29 July 2017

title

Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia (English)

1 reference

29 July 2017

0 references

Neerman-Arbez M

1

1 reference

29 July 2017

Honsberger A

series ordinal

2

1 reference

29 July 2017

Antonarakis SE

series ordinal

3

1 reference

29 July 2017

Morris MA

series ordinal

4

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 January 1999

1 reference

Journal of Clinical Investigation

29 July 2017

published in

1 reference

29 July 2017

volume

103

1 reference

29 July 2017

issue

2

1 reference

29 July 2017

page(s)

215-218

1 reference

Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Congenital dysfibrinogenemia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

CENSOR--a program for identification and elimination of repetitive elements from DNA sequences

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Mutation in blood coagulation factor V associated with resistance to activated protein C.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

MIRs are classic, tRNA-derived SINEs that amplified before the mammalian radiation

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Analysis of fibrinogen genes in patients with congenital afibrinogenemia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

The deletion in a type of δ0-β0-thalassaemia begins in an inverted AluI repeat

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Mutation in LDL receptor: Alu-Alu recombination deletes exons encoding transmembrane and cytoplasmic domains

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Evolution and organization of the fibrinogen locus on chromosome 4: gene duplication accompanied by transposition and inversion

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=407887

Resolution of spontaneous bleeding events but failure of pregnancy in fibrinogen-deficient mice

4 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9916133

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular etiology of factor VIII deficiency in hemophilia A

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9916133

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Fibrinogen Otago: a major alpha chain truncation associated with severe hypofibrinogenaemia and recurrent miscarriage

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9916133

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1172/JCI5471

1 reference

29 July 2017

1 reference

29 July 2017

1 reference