Publisher
Springer Science and Business Media LLC
Reference37 articles.
1. Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J et al (2020) Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis, and extensive cortical malformations. Eur J Med Genet 63(1):103624
2. Chatron N, Cabet S, Alix E, Buenerd A, Cox P, Guibaud L et al (2019) A novel lethal recognizable polymicrogyric syndrome caused by ATP1A2 homozygous truncating variants. Brain 142(11):3367–3374
3. Isaksen TJ, Lykke-Hartmann K (2016) Insights into the Pathology of the α2-Na(+)/K(+)-ATPase in Neurological Disorders. Lessons from Animal Models Front Physiol 7:161
4. Shull MM, Pugh DG, Lingrel JB (1989) Characterization of the human Na, K-ATPase alpha 2 gene and identification of intragenic restriction fragment length polymorphisms. J Biol Chem 264(29):17532–17543
5. Fedosova NU, Habeck M, Nissen P (2021) Structure and Function of Na K-ATPase-The Sodium-Potassium Pump. Compr Physiol 12(1):2659–2679