𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular defects of the C7 gene in two patients with complement C7 deficiency

✍ Scribed by Sonia Barroso; Claudine Rieubland; Antonia JoséÁlvarez; Margarita López-Trascasa; Pierre-Alexandre Bart; Antonio Núñez-Roldán; Berta Sánchez

Book ID
108781870
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
237 KB
Volume
118
Category
Article
ISSN
0019-2805

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

DNA polymorphism of the human complement
DNA polymorphism of the human complement component C7 gene in familial deficiencies
✍ Eliecer Coto; Eduardo Martínez-Naves; Orlando Domínguez; Carlos López-Larrea 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 207 KB

A C7 cDNA probe detecting a TaqI restriction fragment length polymorphism has been used to examine the segregation of the "silent allele" (C7\*Q0) in two familial deficiencies. Carrier diagnosis in healthy children is possible when both parents are heterozygotes. Only one of these two families was i

Deficiency of c7 with systemic lupus ery
Deficiency of c7 with systemic lupus erythematosus. solubilization of immune complexes in complement-deficient sera
✍ Howard J Zeitz; Gary W Miller; Thomas F Lint; Mir A Ali; Henry Gewurz 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 618 KB

## Abstract A woman with systemic lupus erythematosus (SLE) was found to have undetectable serum total complement (C) activity with marked reductions in levels of several C components. Recognition of rising C4, C3, and C5 levels coupled with sustained absence of hemolytic activity led to studies of