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Molecular basis of hereditary C1q deficiency
scientific article
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Statements
instance of
scholarly article
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review article
1 reference
stated in
Europe PubMed Central
title
Molecular basis of hereditary C1q deficiency
(English)
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main subject
Complement C1q C chain
1 reference
stated in
GOA release 2020-03-11
immune response
1 reference
stated in
GOA release 2020-03-11
author name string
F Petry
series ordinal
1
author given names
F
author last names
Petry
1 reference
stated in
PubMed
PubMed publication ID
9777412
retrieved
7 February 2023
language of work or name
English
0 references
publication date
August 1998
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published in
Immunobiology
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volume
199
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issue
2
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page(s)
286-94
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cites work
Localization of the gene cluster encoding the A, B, and C chains of human C1q to 1p34.1-1p36.3
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0171-2985%2898%2980033-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple identification of a particular type of hereditary C1q deficiency in the Turkish population: review of the cases and additional genetic and functional analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0171-2985%2898%2980033-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development of systemic lupus erythematosus in a patient with selective complete C1q deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0171-2985%2898%2980033-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0171-2985%2898%2980033-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0171-2985%2898%2980033-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q: parallels and differences to other known genetic C1q-defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0171-2985%2898%2980033-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complete functional C1q deficiency associated with systemic lupus erythematosus (SLE)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0171-2985%2898%2980033-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0171-2985(98)80033-8
0 references
Fatcat ID
release_sog6hd65lbfkphzmmgzy2ow2ui
0 references
PubMed publication ID
9777412
0 references
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