Maïa Cassard
Maïa Cassard is a young girl with a rare KCNB1 gene mutation that has led to developmental delays and severe epilepsy. Despite her health challenges, she is a source of inspiration and hope for her family and the community involved in KCNB1 research.
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Monaco:
Maïa is a child affected by a rare mutation of the KCNB1 gene, leading to severe developmental delays and epilepsy.
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