Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes
KE Lohmueller, T Sparsø, Q Li, E Andersson… - The American Journal of …, 2013 - cell.com
It has been hypothesized that, in aggregate, rare variants in coding regions of genes explain
a substantial fraction of the heritability of common diseases. We sequenced the exomes of …
a substantial fraction of the heritability of common diseases. We sequenced the exomes of …
[PDF][PDF] Kirk E. Lohmueller, Thomas Sparsø, 2, 18 Qibin Li, 3 Ehm Andersson, 2 Thorfinn Korneliussen, 4 Anders Albrechtsen, 5 Karina Banasik, 2 Niels Grarup, 2 …
M DeGiorgio, T Jørgensen, A Sandbæk… - The American Journal …, 2013 - core.ac.uk
It has been hypothesized that, in aggregate, rare variants in coding regions of genes explain
a substantial fraction of the heritability of common diseases. We sequenced the exomes of …
a substantial fraction of the heritability of common diseases. We sequenced the exomes of …
Facteurs prédictifs de récidive et de sévérité du syndrome hémolytique et urémique atypique et de la glomérulonéphrite à C3 après transplantation rénale
MLQ Donnette-Le Quintrec - 2013 - theses.hal.science
Le syndrome hémolytique et urémique atypique (SHU) et les glomérulonéphrites à dépôts
de C3 sont des pathologies rares. Le SHU atypique est une pathologie aigüe sévère …
de C3 sont des pathologies rares. Le SHU atypique est une pathologie aigüe sévère …