Cite
HARVARD Citation
Ijaz, A. et al. (2019). XPC gene mutations in families with xeroderma pigmentosum from Pakistan; prevalent founder effect. Congenital anomalies. pp. 18-21. [Online].
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Ijaz, A. et al. (2019). XPC gene mutations in families with xeroderma pigmentosum from Pakistan; prevalent founder effect. Congenital anomalies. pp. 18-21. [Online].