(Q33676915)

English

C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.

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scholarly article

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Europe PubMed Central

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21 September 2019

C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3260957%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1

1 reference

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21 September 2019

author name string

S Koskimies

2

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21 September 2019

E Johansson

3

1 reference

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21 September 2019

language of work or name

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publication date

1 June 1988

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21 September 2019

Journal of Medical Genetics

1 reference

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21 September 2019

25

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21 September 2019

6

1 reference

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21 September 2019

387-391

1 reference

Europe PubMed Central

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21 September 2019

Inherited structural polymorphism of the fourth component of human complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

The structural basis of the multiple forms of human complement component C4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Complement deficiency states and infection: epidemiology, pathogenesis and consequences of neisserial and other infections in an immune deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

The role of complement and its receptor in the elimination of immune complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Definitive RFLPs to distinguish between the human complement C4A/C4B isotypes and the major Rodgers/Chido determinants: application to the study of C4 null alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Subacute cutaneous lupus erythematosus: a cutaneous marker for a distinct lupus erythematosus subset

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

21 June 2018

Statement on the nomenclature of human C4 allotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050506

30 October 2018

Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/3260957

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA antigens and complotypes in insulin-dependent diabetes mellitus

1 reference

https://pubmed.ncbi.nlm.nih.gov/3260957

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human MHC class III genes, Bf and C4. Polymorphism, complotypes and association with MHC class I genes in the Finnish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/3260957

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA polymorphism of human HLA-linked complement C4 allotypes, including C4 null alleles, in the Finnish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/3260957

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-A,B,C and haplotype frequencies in the Finnish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/3260957

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.25.6.387

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3260957%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3260957%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3260957%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

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