Lv22
178 积分 2023-10-31 加入
Genotypes and Phenotypes of Chinese Pediatric Patients With Idiopathic and Heritable Pulmonary Arterial Hypertension-A Single-Center Study
21小时前
已完结
De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome
4天前
已完结
Metabolomics, sleepiness, and sleep duration in sleep apnea
25天前
已完结
Novel neurofilament light (Nefl) E397K mouse models of Charcot-Marie-tooth type 2E (CMT2E) present early and chronic axonal neuropathy
1个月前
已完结
A lower X-gate in TASK channels traps inhibitors within the vestibule
2个月前
已完结
Drosophila ZIP13 over-expression or transferrin1 RNAi influences the muscle degeneration of Pink1 RNAi by elevating iron levels in mitochondria
2个月前
已完结
Signalling between G-protein-coupled receptors and TASK1 channels
2个月前
已完结
Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disability
3个月前
已完结
Identification of CNTN2 as a genetic modifier of PIGA-CDG in a family with incomplete penetrance and in Drosophila
6个月前
已完结
CELSR1 variants are associated with partial epilepsy of childhood
8个月前
已完结
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