Homozygous hereditary C1q deficiency and
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Jason H. Slingsby; Peter Norsworthy; Glen Pearce; Akshay K. Vaishnaw; Helen Issl
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Article
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1996
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John Wiley and Sons
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English
⚖ 739 KB
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