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A further case of hereditary C1q-deficiency in a Turkish family from the Netherlands: Analysis of the defected gene and mRNA

✍ Scribed by F. Petry; P.J. Kabel; J. Draaisma; M.R. Daha; M. Loos


Book ID
117326390
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
371 KB
Volume
35
Category
Article
ISSN
0161-5890

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Homozygous hereditary C1q deficiency and
✍ Jason H. Slingsby; Peter Norsworthy; Glen Pearce; Akshay K. Vaishnaw; Helen Issl πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 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