换一批Atypical presentation of <i>SLC30A10</i> gene mutation with hypermanganesemia, seizures and polycythemia.
第一作者：
Spoorthi,Jagadish
第一单位：
Department of Pediatric Neurology, University of Iowa, United States.
作者：
关键词
ADHD, attention deficit hyperactivity disorderALT, alanine transaminaseAST, aspartate transaminaseCBC, complete blood countDystoniaEEG, electroencephalogramHypermanganesemiaMCH, mean corpuscular hemoglobinMCHC, mean corpuscular hemoglobin concentrationMCV, mean corpuscular volumeMRI, magnetic resonance imagingMn, ManganesePolycythemiaRDW, red cell distribution widthSLC30A10 gene mutationSeizuresT1 hyperintensityTIBC, total iron binding capacity
DOI
10.1016/j.ebr.2021.100505
PMID
34877518
发布时间
2021-12-11
- 浏览0
Epilepsy & behavior reports
2021年16卷
100505页
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