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NIPA2mutations are correlative with childhood absence epilepsy in the Han Chinese population

✍ Scribed by Jiang, Yuwu; Zhang, Yuehua; Zhang, Pingping; Zhang, Feng; Xie, Han; Chan, Piu; Wu, Xiru

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

NIPA2located in 15q11.2 is mutated in pa

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CACNA1I Is Not Associated With Childhood

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Common Polymorphisms in the CACNA1H Gene

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The gene encoding GABBR1 is not associat

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Mutation screen of the gene encodingGABR

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T-type calcium channel gene alpha (1G) i

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