Associated Papers
Association Analysis of Rare CNTN5 Variants With Autism Spectrum Disorder in a Japanese Population.
Hadi AF et al.
Neuropsychopharmacology Reports, 2025
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
Zhou Y et al.
Bmc Medical Genetics, 2020
32682410 (PubMed )
Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL3
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