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    Biallelic Mutations in ADAM22 Presenting as Ohtahara Syndrome in an Indian Family: Expanding the Electroclinical Phenotype of ADAM22-Related Neurologic Disorder

    Biallelic Mutations in ADAM22 Presenting as Ohtahara Syndrome in an Indian Family: Expanding the Electroclinical Phenotype of ADAM22-Related Neurologic Disorder by Prateek Kumar Panda, Achanya Palayullakandi, Diksha Gupta, Suthiraj Sopanam, Anand Santosh Mishra, Indar Kumar Sharawat

    Published 2025-03-01
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