Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1.
Auris, nasus, larynx 2016 Mar .
Minami Shujiro B, Mutai Hideki, Namba Kazunori, Sakamoto Hirozazu, Matsunaga Tats
Platelet GPIaC807T polymorphism is associated with negative outcome of sudden hearing loss.
Hearing research 2004 May 191 (1-2): 41-8.
Rudack C, Langer C, Junker R