Associated Papers
Novel variants in ZNF462 and phenotype update in patients with Weiss-Kruszka syndrome: a case series.
Huai W et al.
Translational Pediatrics, 2025
Clinical and Molecular Landscape of Weiss-Kruszka Syndrome: A Case Report and Literature Review.
Li L et al.
Journal of Clinical Research in Pediatric Endocrinology, 2025
Seven Novel Variants of Weiss-Kruszka Syndrome and Phenotype Expansion.
Hau A et al.
American Journal of Medical Genetics. Part A, 2025
A Nonsense Variant of ZNF462 Gene Associated With Weiss-Kruszka Syndrome-Like Manifestations: A Case Study and Literature Review.
Zhao S et al.
Frontiers in Genetics, 2022
Case report: A heterozygous mutation in ZNF462 leads to growth hormone deficiency.
Zhou Y et al.
Frontiers in Genetics, 2022
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