Cite
HARVARD Citation
Philip, N. et al. (2003). Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia. Journal of medical genetics. 40 (6), pp. 441-446. [Online].
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Philip, N. et al. (2003). Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia. Journal of medical genetics. 40 (6), pp. 441-446. [Online].