𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Rare β-thalassemia mutations are cause of concern

✍ Scribed by Anju Gupta; Sarita Agarwal


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
84 KB
Volume
76
Category
Article
ISSN
0361-8609

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


NTNG1 mutations are a rare cause of Rett
✍ Hayley L. Archer; Julie C. Evans; David S. Millar; Peter W. Thompson; Alison M. 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 86 KB 👁 1 views
Initiation codon mutation (ATG → ATA) of
✍ Dr. Britta Landin; Olle Rudolphi; BÖRje Ek 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 436 KB 👁 1 views

An initiation codon mutation ATG-ATA of the p-globin gene was found in seven members of three generations of a family living in northern Sweden. This mutation, which has not previously been described, changes the initiation codon for methionine into a codon for isoleucine and will then result in a p