Published in
Wiley, The American Journal of Medical Genetics - Part A, 3(176), p. 676-681, 2018
DOI: 10.1002/ajmg.a.38592
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Bi-allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus
Journal article published in 2018 by
Gaia Ruggeri,
Andrew E. Timms,
Chi Cheng,
Avery Weiss,
Peter Kollros,
Teresa Chapman,
Hannah Tully,
Ghayda M. Mirzaa 
This paper is available in a repository.
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