(Q28576451)

6

0 references

author name string

G. Jayandharan

1

1 reference

31 January 2017

A. Viswabandya

3

1 reference

31 January 2017

M. Chandy

4

1 reference

31 January 2017

A. Srivastava

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

5

1 reference

31 January 2017

1 July 2007

1 reference

31 January 2017

1 reference

31 January 2017

13

1 reference

31 January 2017

4

1 reference

31 January 2017

413–419

1 reference

31 January 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2516.2007.01477.X

Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2516.2007.01477.X

The comparative role of consanguinity in infant and childhood mortality in Pakistan

21 April 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Recessively inherited coagulation disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

A mutation in LMAN1 (ERGIC-53) causing combined factor V and factor VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Combined deficiency of factor V and factor VIII is due to mutations in either LMAN1 or MCFD2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Molecular characterization of the ERGIC-53 gene in two Japanese patients with combined factor V-factor VIII deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Combined factor V and factor VIII deficiency in a Thai patient: a case report of genotype and phenotype characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Haemorrhagic symptoms in patients with combined factors V and VIII deficiency in north-eastern Iran

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Combined factor V and VIII deficiency: a new family and their haemorrhagic manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Combined factor V and VIII deficiency in Indian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

Decreased factor VIII clotting antigen levels in the combined factor V and VIII deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2007.01477.X

10.1111/J.1365-2516.2007.01477.X

21 January 2018

Identifiers

DOI

1 reference

31 January 2017

release_r7rohep735h4lp4w27usrgu47i

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/r7rohep735h4lp4w27usrgu47i