WDR47, involved in microtubule dynamics and function, is a candidate gene for heterotaxy syndrome July 4, 2018 No Comments
Loss-of-function mutation in TCF12 gene linked to autosomal dominant Kallmann syndrome June 21, 2018 No Comments
ITGB3 gene polymorphism is positively associated with pericellular fibrosis in patients with NAFLD June 13, 2018 No Comments
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