Literature DB >> 34014491

Expanding phenotype of ATP1A3 mutation.

Ajith Cherian1, J Nandana1, K P Divya2, Sharath Chandra Shetty1.   

Abstract

Entities:  

Year:  2021        PMID： 34014491     DOI： 10.1007/s13760-021-01706-1

Source DB:  PubMed          Journal:  Acta Neurol Belg        ISSN： 0300-9009            Impact factor:   2.396


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  1 in total

1.  Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow-up.

Authors:  Weihua Zhang; Jiuwei Li; Xiuwei Zhuo; Ji Zhou; Weixing Feng; Shuai Gong; Xiaotun Ren; Changhong Ding; Tongli Han; Fang Fang
Journal:  Pediatr Investig       Date:  2022-02-25
  1 in total

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