(Q40998116)

English

Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon

scientific article published on November 1998

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scholarly article

1 reference

Europe PubMed Central

25 September 2017

Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon (English)

1 reference

Europe PubMed Central

25 September 2017

author name string

Fredrikson GN

1

1 reference

Europe PubMed Central

25 September 2017

Gullstrand B

2

1 reference

Europe PubMed Central

25 September 2017

Schneider PM

3

1 reference

Europe PubMed Central

25 September 2017

Witzel-Schlömp K

4

1 reference

Europe PubMed Central

25 September 2017

Sjöholm AG

5

1 reference

Europe PubMed Central

25 September 2017

Alper CA

6

1 reference

Europe PubMed Central

25 September 2017

Awdeh Z

7

1 reference

Europe PubMed Central

25 September 2017

Truedsson L

8

1 reference

Europe PubMed Central

25 September 2017

publication date

1 November 1998

1 reference

Europe PubMed Central

25 September 2017

Human Immunology

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Europe PubMed Central

25 September 2017

59

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Europe PubMed Central

25 September 2017

11

1 reference

Europe PubMed Central

25 September 2017

713-719

1 reference

Europe PubMed Central

25 September 2017

A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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C4B gene polymorphism detected in a human cosmid clone

1 reference

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7 January 2021

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Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants

1 reference

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7 January 2021

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Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genes

1 reference

https://api.crossref.org/works/10.1016%2FS0198-8859%2898%2900068-8

7 January 2021

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The dichotomous size variation of human complement C4 genes is mediated by a novel family of endogenous retroviruses, which also establishes species-specific genomic patterns among Old World primates

1 reference

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7 January 2021

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Polymorphism of human complement component C4.

1 reference

https://api.crossref.org/works/10.1016%2FS0198-8859%2898%2900068-8

7 January 2021

based on heuristic

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C4 Reference Typing Report

1 reference

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Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic model

1 reference

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7 January 2021

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Genetic polymorphism of the fourth component of human complement: population study and proposal for a revised nomenclature based on genomic PCR typing of Rodgers and Chido determinants.

1 reference

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7 January 2021

based on heuristic

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Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus

1 reference

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Amino acid sequence around the thiol and reactive acyl groups of human complement component C4.

1 reference

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based on heuristic

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Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity.

1 reference

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Infectious diseases associated with complement deficiencies

1 reference

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based on heuristic

inferred from DOI database lookup

Molecular basis of complete C4 deficiency. A study of three patients

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression

1 reference

https://api.crossref.org/works/10.1016%2FS0198-8859%2898%2900068-8

7 January 2021

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Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family

1 reference

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7 January 2021

based on heuristic

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Homozygous deficiency of C4 in a child with a lupus erythematosus syndrome

1 reference

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7 January 2021

based on heuristic

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'Touchdown' PCR to circumvent spurious priming during gene amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0198-8859%2898%2900068-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Complotypes and extended haplotypes in laboratory medicine

1 reference

https://api.crossref.org/works/10.1016%2FS0198-8859%2898%2900068-8

7 January 2021

based on heuristic

inferred from DOI database lookup

New DNA sequences for the human complement gene C4.

1 reference

https://api.crossref.org/works/10.1016%2FS0198-8859%2898%2900068-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Restriction fragment analysis of non-deleted complement C4 null genes suggests point mutations in C4A null alleles, but gene conversions in C4B null alleles

1 reference

https://api.crossref.org/works/10.1016%2FS0198-8859%2898%2900068-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0198-8859(98)00068-8

1 reference

Europe PubMed Central

25 September 2017

1 reference

Europe PubMed Central

25 September 2017

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