Cite
HARVARD Citation
Olinger, E. et al. (2021). A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families. Human mutation. 42 (10), pp. 1221-1228. [Online].
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Olinger, E. et al. (2021). A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families. Human mutation. 42 (10), pp. 1221-1228. [Online].