Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus

Gaia Ruggeri, Andrew E. Timms, Chi Cheng, Avery Weiss, Peter Kollros, Teresa Chapman, Hannah Tully, Ghayda M. Mirzaa
  • American Journal of Medical Genetics Part A, January 2018, Wiley
  • DOI: 10.1002/ajmg.a.38592
The author haven't yet claimed this publicationThe author haven't yet claimed this publication

In partnership with: