@dpavot:30535804 / 11-30
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Although a digenic inheritance pattern of hearing impairment has been reported for heterozygous missense variants of ATP2B2 and CDH23, our findings indicate a monogenic cause of hearing impairment in cases with loss-of-function variants of ATP2B2.
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projects
| Unselected / annnotation | Selected / annnotation | |
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