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A) mutations identified in family YF-KHZ with hearing loss.
A) Pedigree of the YK1132 family, presenting the segregation of the c.577A>C mutation. B) Validation of EYA1 deletion by Real-time CQ-PCR. The relative quantity of Introns 1 in the Patient was almost half of the patient’s father and mother. Values are expressed as the mean ± standard error
