https://www.selleckchem.com/pr....oducts/pf-9363-ctx-6
919-2AG) was recurrent and accounted for 31% of all mutant alleles. One out of 7 (14.3%) families with mutations were confirmed to be Pendred syndrome (PS). The SLC26A4 mutations have a high carrying rate in ARNSHL Iranian patients. The identification of a disease causing mutation can be used to establish a genotypic diagnosis and provide important information to the patients and their families.Electronic Health Records (EHRs) represent a source of high value data which is often underutilized because exploiting the informati
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