Associated Papers
NHE9 and Endosomal pH: Converging Mechanisms in Neurodevelopmental, Psychiatric and Neurodegenerative Disorders.
Prasad H
The European Journal of Neuroscience, 2025
Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family.
Yang D et al.
Frontiers in Genetics, 2021
34603379 (PubMed )
Supplement: Data_Sheet_1.XLSX › DX1616_21D03390594-1
Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission.
Al-Mubarak BR et al.
European Journal of Human Genetics : Ejhg, 2020
Functional analysis of Na+/H+ exchanger 9 variants identified in patients with autism and epilepsy.
Prasad H et al.
Matters, 2017
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