The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients-Reference-Cited by-同舟云学术

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The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients

Published:2023-09 Issue:8 Volume:45 Page:422-431
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Dai Lifang,Ding Changhong,Tian Xiaojuan,Liu Ming,Ma Yuping,Chen Chunhong,Ren Xiaotun,Li Hua

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference24 articles.

1. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2;De Fusco;Nat Genet,2003

2. Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation;Swoboda;Ann Neurol,2004

3. ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria;Vetro;Brain,2021

4. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations;Monteiro;Eur J Med Genet,2020

5. Diagnostic and therapeutic aspects of hemiplegic migraine;Di Stefano;J Neurol Neurosurg Psychiatry,2020

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