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Open Accesshttps://doi.org/10.4103/aian.aian_706_24
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Cite Publication Date: Jan 8, 2025 | |
 License type: cc-by-nc-sa |
Biallelic Mutations in ADAM22 Presenting as Ohtahara Syndrome in an Indian Family: Expanding the Electroclinical Phenotype of ADAM22-Related Neurologic Disorder.
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