Lv1
78 积分 2025-04-12 加入
Novel mutation in EFEMP1 identified from two Chinese POAG families differentially activated endoplasmic reticulum stress markers and induced glaucoma in mouse
3小时前
待确认
Reproducible stimulation of ciliary muscle contraction in the cynomolgus monkey via a permanent indwelling midbrain electrode
6天前
已完结
Mechanisms underlying phenotypic variation in neurogenetic disorders
23天前
已完结
The Role of hsa-miR-548l Dysregulation as a Putative Modifier Factor for Glaucoma-Associated FOXC1 Mutations
1个月前
已完结
Screening for Mutations of Axenfeld-Rieger Syndrome Caused by FOXC1 Gene in Japanese Patients
1个月前
已完结
Autosomal recessive congenital hereditary corneal dystrophy associated with a novel SLC4A11 mutation in two consanguineous Tunisian families
1个月前
已完结
A review of the role of EFEMP1 in ophthalmic disease
2个月前
已关闭
Chorioretinopathy presenting as bitemporal hemianopia
2个月前
已关闭
Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome
2个月前
已完结
Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes
2个月前
已完结
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