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De novo R853Q mutation of SCN2A gene and West syndrome.
Samanta D, Ramakrishnaiah R. De novo R853Q mutation of SCN2A gene and West syndrome. Acta Neurol Belg. 2015 Dec; 115(4):773-6.
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PubMed
subject areas
Arginine
Glutamine
Humans
Infant
Male
Mutation
NAV1.2 Voltage-Gated Sodium Channel
Spasms, Infantile
authors with profiles
Raghu Hosahalli Ramakrishnaiah
Debopam Samanta
De novo R853Q mutation of SCN2A gene and West syndrome.