𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Hyperlipoproteinaemia(a) is a common cause of autosomal dominant hypercholesterolaemia

✍ Scribed by E. Meriño-Ibarra; J. Puzo; E. Jarauta; A. Cenarro; D. Recalde; Á. L. García-Otín; E. Ros; E. Martorell; X. Pintó; M. Franco; D. Zambón; Á. Brea; M. Pocoví; F. Civeira


Publisher
Springer
Year
2007
Tongue
English
Weight
308 KB
Volume
30
Category
Article
ISSN
0141-8955

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Mutations of the EPHA2 receptor tyrosine
✍ Tianxiao Zhang; Rui Hua; Wei Xiao; Kathryn P. Burdon; Shomi S. Bhattacharya; Jam 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 520 KB

Congenital cataracts (CCs) are clinically and genetically heterogeneous. Mutations in the same gene may lead to CCs differing in inheritance, morphology and severity. Loci for autosomal dominant posterior polar CC and total CC have both been mapped to the chromosomal 1p36 region harboring the EPHA2