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110 积分 2023-08-12 加入
DEAD/DEAH-box RNA helicases shape the risk of neurodevelopmental disorders
1天前
已完结
ADAR1 and its implications in cancer development and treatment
1天前
已完结
Methylated GCC repeat expansion in AFF3 associates with intellectual disability
3天前
已完结
GABAergic Interneuron Dysfunction in Neurodevelopmental Disorders: A New Role for the Transcription Factor MEF2C in Regulating Parvalbumin Interneuron Survival and Function
5天前
已完结
Experience-dependent maturation of somatosensory parvalbumin interneurons during social development in prairie voles
5天前
已完结
Fatal encephalopathy and congenital heart defects with MEF2C ‐related disorder
5天前
已完结
De Novo Chromosomes 3q and 5q Chromothripsis Leads to a 5q14.3 Microdeletion Syndrome Presentation: Case Report and Review of the Literature
5天前
已完结
De novo 5q14.3 translocation 121.5‐kb upstream of MEF2C in a patient with severe intellectual disability and early‐onset epileptic encephalopathy
5天前
已完结
5q14.3 neurocutaneous syndrome: A novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2C
5天前
已完结
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