Cite
HARVARD Citation
Evers, C. et al. (2016). Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy. American journal of medical genetics. 170 (6), pp. 1502-1509. [Online].
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Evers, C. et al. (2016). Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy. American journal of medical genetics. 170 (6), pp. 1502-1509. [Online].