Last Updated：2025/11/27
Researchers identified a novel mutation associated with Opitz-Kaveggia syndrome in a family with developmental delay.
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Researchers identified a novel mutation associated with Opitz-Kaveggia syndrome in a family with developmental delay.
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研究者たちは発達遅滞のある家族で、FG症候群に関連する新規変異を同定しました。
