CHU Sainte-Justine Research Center

Québec siblings with rare orphan disease lead to discovery of rare genetic diseases

Published: 25Apr2019

Mutations in a gene involved in brain development have led to the discovery of two new neurodevelopmental diseases by an international team led by researchers at McGill University and CHU Sainte...

Identification of a new gene causing scoliosis and bone malformations

Published: 2Nov2017

A unique collaboration among Shriners Hospital for Children – Canada, CHU Sainte-Justine and McGill University has enabled researchers to identify genetic mutations involved in a rare disease that...