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10 积分 2024-05-06 加入
Loss-of-function SLC25A20 mutation causes carnitine-acylcarnitine translocase deficiency by reducing SLC25A20 protein stability
6小时前
已完结
A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K/AKT/mTOR signaling pathway
6小时前
已完结
The loss of function GBA1 c.231C > G mutation associated with Parkinson disease
7小时前
已完结
Amelogenesis imperfecta: More than just an enamel problem
9个月前
已完结
Molecular‐based phenotype variations in amelogenesis imperfecta
9个月前
已完结
Mesenchymal condensation in tooth development and regeneration: a focus on translational aspects of organogenesis
9个月前
已完结
Midkine Promotes Odontoblast-like Differentiation and Tertiary Dentin Formation
9个月前
已完结
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