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
Mutation analysis of WNT10B in obese children, adolescents and adults.
Van Camp JK et al.
Endocrine, 2013
A functional promoter polymorphism -607G>C of WNT10B is associated with abdominal fat in Korean female subjects.
Kim IC et al.
The Journal of Nutritional Biochemistry, 2011
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