Identifies the genetic link between sensorineural hearing loss and renal tubular acidosis, indicating new pathways for understanding Pendred syndrome.
This study aims to provide new insights in understanding the genetic association between sensorineural hearing loss with distal renal tubular acidosis (RTA) and to add ATP6V1B1 to the list of known genes causing "Pendred ear phenotype".
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Prasad et al. (2026) studied this question.
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