Associated Papers
Clinical and genetic diagnosis of a patient with focal segmental glomerulosclerosis due to a novel variant of the ANLN gene.
Zhang J et al.
Cen Case Reports, 2026
Identification of ANLN as a new likely pathogenic gene of branchio-otic syndrome in a three-generation Chinese family.
Deng L et al.
Molecular Genetics & Genomic Medicine, 2019
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