Cite
HARVARD Citation
Hashmi, J. et al. (2018). Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. Congenital anomalies. pp. 10-15. [Online].
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Hashmi, J. et al. (2018). Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa. Congenital anomalies. pp. 10-15. [Online].