Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies (Q92800385)

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1 May 2020

title

Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies (English)

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Véronique Frémeaux-Bacchi

1 May 2020

author

object named as

Véronique Frémeaux-Bacchi

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1 May 2020

Carine El Sissy

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1 May 2020

Jérémie Rosain

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1 May 2020

Paula Vieira-Martins

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1 May 2020

Pauline Bordereau

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1 May 2020

Aurélia Gruber

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1 May 2020

Magali Devriese

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1 May 2020

Loïc de Pontual

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1 May 2020

Muhamed-Kheir Taha

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1 May 2020

Claire Fieschi

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1 May 2020

Capucine Picard

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1 May 2020

publication date

8 August 2019

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1 May 2020

published in

Frontiers in Immunology

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1 May 2020

volume

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1 May 2020

page(s)

1936

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Creative Commons Attribution 4.0 International

1 May 2020

start time

8 August 2019

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April 2022 Public Data File from Crossref

copyrighted

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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11 February 2021

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High prevalence of complement C7 deficiency among healthy blood donors of Moroccan Jewish ancestry

11 February 2021

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Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies

11 February 2021

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Properdin deficiency: molecular basis and disease association

11 February 2021

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The molecular basis of C6 deficiency in the western Cape, South Africa

11 February 2021

1 reference

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Human properdin deficiency has a heterogeneous genetic background

11 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6694794

Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism

11 February 2021

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Inherited deficiencies of the terminal complement components

11 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6694794

Complete and partial deficiencies of complement factor D in a Dutch family

11 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6694794

Infectious diseases associated with complement deficiencies

11 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6694794

Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing

11 February 2021

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=6694794

11 February 2021

Identifiers

DOI

10.3389/FIMMU.2019.01936

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31440263%20AND%20SRC:MED&resulttype=core&format=json

1 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31440263%20AND%20SRC:MED&resulttype=core&format=json

1 May 2020

PubMed publication ID

31440263

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31440263%20AND%20SRC:MED&resulttype=core&format=json