OBO ID: DOID:0110484

Citations

(1 total)

Term: autosomal recessive nonsyndromic deafness 26

Yousaf, R., Ahmed, Z.M., Giese, A.P., Morell, R.J., Lagziel, A., Dabdoub, A., Wilcox, E.R., Riazuddin, S., Friedman, T.B., Riazuddin, S. (2018) Modifier variant of METTL13 suppresses human GAB1-associated profound deafness. The Journal of Clinical Investigation. 128(4):1509-1522