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
40949918 (PubMed )
Supplement: tp-14-08-1991-supplementary.pdf
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
Empty Sella Syndrome Associated with Growth Hormone Deficiency: the First Case Report of Weiss-Kruszka Syndrome.
Park J et al.
Journal of Korean Medical Science, 2021
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