Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

Overview of attention for article published in Orphanet Journal of Rare Diseases, May 2014

Altmetric Badge

Mentioned by

So far, Altmetric has seen 1 public wall post.

Dr. Enza Maria Valente and her team has published an article Noting B9D1 and MKS1 as JS causative genes increasing our JS…

This page shows the most recent Facebook posts that mention this research output.

Click here to find out how to access more activity.