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

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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. | LitMetric

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

Prateek Kumar Panda Achanya Palayullakandi Diksha Gupta Suthiraj Sopanam Anand Santosh Mishra Indar Kumar Sharawat

Ann Indian Acad Neurol

Pediatric Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.

Published: January 2025

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http://dx.doi.org/10.4103/aian.aian_706_24 DOI Listing

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