Pseudohypoaldosteronism Type II Caused by CUL3 Mutation Presented with Visual Impairment
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DOI: 10.4103/0366-6999.237397
Abstract: To the Editor: Pseudohypoaldosteronism Type II (PHAII), also known as Gordon syndrome, is a rare autosomal disease, caused by mutations in WNK1, WNK4, CUL3, or KLHL3 genes. Hitherto, about 200 individuals and families have been… read more here.
Keywords: caused cul3; pseudohypoaldosteronism type; cul3 mutation;