Associated Papers
A novel mutation in TRIOBP gene leading to congenital deafness in a Chinese family.
Zhou B et al.
Bmc Medical Genetics, 2020
Whole exome sequencing identifies TRIOBP pathogenic variants as a cause of post-lingual bilateral moderate-to-severe sensorineural hearing loss.
Pollak A et al.
Bmc Medical Genetics, 2017
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