Meckel-Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances

Meckel-Gruber syndrome (MKS) is a lethal autosomal recessive congenital anomaly syndrome caused by mutations in genes encoding proteins that are structural or functional components of the primary cilium. Conditions that are caused by mutations in ciliary genes are collectively termed the ciliopathie...

Full description

Saved in:
Bibliographic Details
Main Authors: Verity Hartill (Author), Katarzyna Szymanska (Author), Saghira Malik Sharif (Author), Gabrielle Wheway (Author), Colin A. Johnson (Author)
Format: Book
Published: Frontiers Media S.A., 2017-11-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available