Cite
HARVARD Citation
Ruggeri, G. et al. (2018). Bi‐allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus. American journal of medical genetics. 176 (3), pp. 676-681. [Online].
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Ruggeri, G. et al. (2018). Bi‐allelic mutations of CCDC88C are a rare cause of severe congenital hydrocephalus. American journal of medical genetics. 176 (3), pp. 676-681. [Online].