Citations for
1DFNB97, MET
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
Mujtaba G, Schultz JM, Imtiaz A, Morell RJ, Friedman TB, Naz S.
J Med Genet. Aug;52(8):548-52. doi: 10.1136/jmedgenet-2015-103023. Epub 2015 May 4. 2015