Novel α-galactosidase A gene mutation in a Chinese Fabry disease family: A case report

doi:10.12998/wjcc.v10.i3.1067

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Jan 21, 2022 (publication date) through Nov 25, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Jan 21, 2022; 10(3): 1067-1076
Published online Jan 21, 2022. doi: 10.12998/wjcc.v10.i3.1067

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Figure 4 Light microscopy of renal biopsy (periodic acid-Schiff staining, 400 ×) showing membranous nephropathy. Heterogeneous thickening of the glomerular capillary basement membrane is visible.

Citation: Fu AY, Jin QZ, Sun YX. Novel α-galactosidase A gene mutation in a Chinese Fabry disease family: A case report. World J Clin Cases 2022; 10(3): 1067-1076
URL: https://www.wjgnet.com/2307-8960/full/v10/i3/1067.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i3.1067