Rossanti, R., Watanabe, T., Nagano, C., Hara, S., Horinouchi, T., Yamamura, T., . . . Nozu, K. (2020). FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child. CEN Case Rep.
Citação norma ChicagoRossanti, Rini, et al. "FAT1 Biallelic Truncating Mutation Causes a Non-syndromic Proteinuria in a Child." CEN Case Rep 2020.
MLA CitationRossanti, Rini, et al. "FAT1 Biallelic Truncating Mutation Causes a Non-syndromic Proteinuria in a Child." CEN Case Rep 2020.
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