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Springer Science and Business Media LLC
Reference44 articles.
1. Allocco AA, Jin SC, Duy PQ, Furey CG, Zeng X, Dong W et al (2019) Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3. Front Cell Neurosci 26(13):425–425
2. Alyamani SA, Aldhalaan HM, Almuhaizea MA, Abukhalid MF (2023) Expanding the Allelic spectrum in ATP1A3-related disorders with 3 novel mutations and clinic features. Neurosciences (riyadh) 28(3):195–198
3. Arystarkhova E, Haq IU, Luebbert T, Mochel F, Saunders-Pullman R, Bressman SB et al (2019) Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition. Neurobiol Dis 1:132
4. Ben YT, Benrhouma H, Klaa H, Rouissi A, Chaabouni M, Kraoua I et al (2018) Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review. Neuropediatrics 49(5):339–341
5. Berberich AJ, Ho R, Hegele RA (2018) Whole genome sequencing in the clinic: empowerment or too much information? CMAJ : Canadian Med Assoc J 190(5):E124
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