Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss

Table 1 Summary of the audiological features of affected members of family SH-02

Patient	Gender	Age (years)		Use of aminoglycoside	Hearing test dBHL (PTA)		Verbal function	Level of hearing impairment	Vertigo	Tinnitus	Intelligence
Patient	Gender	At testing	At onset	Use of aminoglycoside	Left ear	Right ear	Verbal function	Level of hearing impairment	Vertigo	Tinnitus	Intelligence
III-4	Female	35	On birth	No	Null	Null	Null	Anacusia	No	No	Normal
III-5	Male	31	On birth	No	Null	Null	Null	Anacusia	No	No	Normal

ISSN: 1479-5876