Cite
HARVARD Citation
Hameed, A. et al. (n.d.). Bioinformatics evaluation of NPHS2 deletion mutation associated with congenital nephrotic syndrome in a consanguineous Pakistani family. Clinical genetics. pp. 599-601. [Online].
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Hameed, A. et al. (n.d.). Bioinformatics evaluation of NPHS2 deletion mutation associated with congenital nephrotic syndrome in a consanguineous Pakistani family. Clinical genetics. pp. 599-601. [Online].