Bi‐allelic mutations of <i>ccdc88c</i> are a rare cause of severe congenital hydrocephalus

DOI: 10.1002/ajmg.a.38592

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Issn Print: 1552-4825

Publication Date: 2018/03/01

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: Center for Integrative Brain Research


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