Cite
HARVARD Citation
Dunn, P. et al. (2017). A de novo splice site mutation in CASK causes FG syndrome‐4 and congenital nystagmus. American journal of medical genetics. 173 (3), pp. 611-617. [Online].
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Dunn, P. et al. (2017). A de novo splice site mutation in CASK causes FG syndrome‐4 and congenital nystagmus. American journal of medical genetics. 173 (3), pp. 611-617. [Online].