DOI: 10.1002/ajmg.a.38592 , PMID: 29341397 Issn Print: 1552-4825 Publication Date: 2018/03/01 Print 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 + Author Information Author Information: Center for Integrative Brain Research Checking for direct PDF access through Ovid View on Journal Site Abstract Abstract unavailable for this article.
