Spedicati B., Morgan A., Faletra F., Feresin A., Pelliccione G., Gasparini P., Girotto G. (2021) "TBC1D24 and non-syndromic autosomal dominant hearing loss: the identification of an additional Italo-American family carrying the p.(S178L) mutation
" Audiologia e Foniatria, 6(1), 4-8. DOI: 10.14658/pupj-IJAP-2021-1-3
Whole Exome Sequencing
Whole Exome Sequencing