黑料不打烊

Qu茅bec siblings with rare orphan disease lead to discovery of rare genetic diseases

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 黑料不打烊 University and CHU Sainte...

• Read more about Qu茅bec siblings with rare orphan disease lead to discovery of rare genetic diseases