Deficiency in FAM20A leads to skeletal and dental defects – a study in FAM20A knockout mice
Family with sequence similarity 20 (FAM20) consists of three members: FAM20A, FAM20B and FAM20C. Mutations in FAM20 family have been linked to developmental disorders involving bones, cartilage and teeth. FAM20A mutations in humans are associated with amelogenesis imperfecta with gingival fibromatos...
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| Language: | en_US |
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2018
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| Online Access: | https://hdl.handle.net/2144/26272 |