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

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|176|3|676-681

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.176, Iss.3, 2018-03, pp. : 676-681

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Abstract