𝔖 Bobbio Scriptorium
✦   LIBER   ✦

13 Mannose binding lectin gene as a modifier of cystic fibrosis phenotype in Argentinian pediatric patients

✍ Scribed by C. Crespo; H. Giugno; L.P. Gravina; A. Mangano; L. Chertkoff; C. Castaños


Book ID
117799524
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
55 KB
Volume
11
Category
Article
ISSN
1569-1993

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Cystic fibrosis patients with mutation 1
✍ V. Nunes; T. Casals; A. Gaona; G. Antiñolo; J. Ferrer-Calvete; J. Pérez-Frias; E 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 437 KB

The majority of the identified cystic fibrosis (CF) mutations are very uncommon in the total patient population, making the correlation between the clinical presentation and the molecular alterations difficult. The largest deletion that has been described so far in C F is of 84 bp in exon 13, which