Publications resulting from Research:
Choi, H.J., Kanwal, S., Hameed, R. Tamanna N, Perveen S, Mahreen H, Son W, Lee KS and Chung KW (2023). Biallelic mutations in Pakistani families with autosomal recessive prelingual nonsyndromic hearing loss. Genes & Genomics, 45:145–156. DOI: https://doi.org/10.1007/s13258-022-01349-3.
Jung, N.Y., Kwon, H.M.; Nam, D.E., Tamanna, N., Lee, A.J., Kim, S.B., Choi, B.-O., and Chung K.W (2022). Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients. Genes, 13(7):1219. DOI: https://doi.org/10.3390/genes13071219
