Pendred Syndrome by SLC26A4 Gene Sequencing*
฿22,190.00
Sequences the SLC26A4 gene to identify variants associated with Pendred syndrome and SLC26A4-related hearing loss.
การใช้งานทั่วไป
Used to investigate suspected inherited sensorineural hearing loss, particularly with an enlarged vestibular aqueduct, thyroid involvement or a relevant family history.
การเตรียมตัว
รายการตรวจที่เกี่ยวข้อง
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