Back to search

Article

Sex-specific and age-related progression of auditory neurophysiological deficits in the <i>Cln3</i> mouse model of Batten disease

2025-03-18

Abstract excerpt

CLN3 disease is a prevalent form of Neuronal Ceroid Lipofuscinosis (NCL) caused by inherited mutations in the CLN3 gene, with symptoms such as vision loss, language impairment, and cognitive decline. The early onset of visual deficits complicates neurological assessment of brain pathophysiology underlying cognitive decline, while the small number of CLN3 mutation cases in humans hinders the study of sex differen...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
b461639f-ca65-50f6-9c31-1a59980541a0
DOI
10.1101/2025.03.18.643722
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Sex-specific and age-related progression of auditory neurophysiological deficits in the <i>Cln3</i> mouse model of Batten diseaseDOI 10.1101/2025.03.18.643722
Select a neighboring publication to make it the new centre.