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Literature DB >> 33207363

Reply: De novo SPTAN1 mutation in axonal sensorimotor neuropathy and developmental disorder.

Liedewei Van de Vondel^1,2, Jonathan Baets^1,2,3, Danique Beijer^1,2.

Abstract

Entities: Disease Gene

Year: 2020 PMID： 33207363 DOI： 10.1093/brain/awaa345

Source DB: PubMed Journal: Brain ISSN： 0006-8950 Impact factor: 13.501

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1. Longitudinal neurodevelopmental profile of a pediatric patient with de novo SPTAN1, epilepsy, and left hippocampal sclerosis.

Authors: C Luongo-Zink; C Ammons; R Al-Ramadhani; R Logan; K E Ono; S Bhalla; A Kheder; D J Marcus; D L Drane; D J Bearden
Journal: Epilepsy Behav Rep Date: 2022-05-08

1 in total