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Molecular and epidemiologic studies on selective complete C1q deficiency in Turkey

✍ Scribed by A.I. Berkel; E. Birben; C. Öner; I. Yeniay; F. Petry; M. Loos


Book ID
117326229
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
342 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 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 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