|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
4
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|
pubmed:dateCreated |
1996-6-25
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|
pubmed:abstractText |
To describe a new kindred with Clq deficiency and to identify the molecular lesions responsible for complete functional C1q deficiency in this and 2 other previously described kindreds.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
AIM
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|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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|
pubmed:month |
Apr
|
|
pubmed:issn |
0004-3591
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
39
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
663-70
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|
pubmed:dateRevised |
2005-11-17
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|
pubmed:meshHeading |
pubmed-meshheading:8630118-Base Sequence,
pubmed-meshheading:8630118-Child, Preschool,
pubmed-meshheading:8630118-Complement C1q,
pubmed-meshheading:8630118-Consanguinity,
pubmed-meshheading:8630118-Female,
pubmed-meshheading:8630118-Gene Deletion,
pubmed-meshheading:8630118-Homozygote,
pubmed-meshheading:8630118-Humans,
pubmed-meshheading:8630118-Infant,
pubmed-meshheading:8630118-Lupus Erythematosus, Systemic,
pubmed-meshheading:8630118-Male,
pubmed-meshheading:8630118-Molecular Sequence Data,
pubmed-meshheading:8630118-Nuclear Family,
pubmed-meshheading:8630118-Point Mutation
|
|
pubmed:year |
1996
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|
pubmed:articleTitle |
Homozygous hereditary C1q deficiency and systemic lupus erythematosus. A new family and the molecular basis of C1q deficiency in three families.
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pubmed:affiliation |
Hammersmith Hospital, London, UK.
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pubmed:publicationType |
Journal Article,
Case Reports
|
