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New C1q mutation in a Tunisian family

✍ Scribed by Jlejla, H.; Kallel-Sellami, M.; Imen, S.; Laadhar, L.; Zerzri, Y.; Gorgi, Y.; Makni, S.

Book ID: 122018291
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 62 KB
Volume: 56
Category: Article
ISSN: 0161-5890
DOI: 10.1016/j.molimm.2013.05.120

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Objective. To describe a new kindred with Clq deficiency and to identify the molecular lesions responsible for complete functional Clq deficiency in this and 2 other previously described kindreds. Methods. The A-, B-, and C-chain genes of Clq were amplified by polymerase chain reaction, cloned, and