Early neural dysfunction reflected in degraded auditory cortex responses in pre-regression heterozygous Mecp2 rats

Rett syndrome, a genetic disorder caused by mutations in the X-linked Mecp2 gene, is characterized by typical early development followed by rapid developmental regression between 6 and 18 months of age. Affected individuals exhibit seizures, cognitive impairments, motor deficits, and difficulties in...

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Үндсэн зохиолчид:	Yuko Tamaoki, Samantha L. Kroon, Brendan M. Williams, Jonathan R. Riley, Crystal T. Engineer
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	Elsevier 2025-06-01
Цуврал:	Neurobiology of Disease
Нөхцлүүд:	Rett syndrome Mecp2 Auditory cortex Sensory processing Neurodevelopmental disorders
Онлайн хандалт:	http://www.sciencedirect.com/science/article/pii/S0969996125001421
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!