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Undiagnosed Rare Disease Clinic Identifies a Novel UBE3A Variant in Two Sisters with Angelman Syndrome: the End of a Diagnostic Odyssey

Rebecca Bruns,Khurram Liaqat,Abdul Nasir,Kayla Treat, Vinaya S. Murthy,Lili Mantcheva, Wilfredo Torres,Erin Conboy,Francesco Vetrini

Congenital Anomalies(2024)

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Angelman syndrome,diagnostic odyssey,genetic imprinting,undiagnosed rare disease clinic
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