Cite
HARVARD Citation
Issler, N. et al. (2022). A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Journal of the American Society of Nephrology. 33 (4), pp. 732-745. [Online].
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Issler, N. et al. (2022). A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Journal of the American Society of Nephrology. 33 (4), pp. 732-745. [Online].