Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › SPK13_het
A familial case of Galloway-Mowat syndrome due to a novel TP53RK mutation: a case report.
Hyun HS et al.
Bmc Medical Genetics, 2018
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