Sox9 reshapes the biliary tree in Alagille syndrome
Alagille syndrome is a rare pediatric genetic disorder that can affect the liver, heart, kidneys, blood vessels, skeleton and other tissues. One major characteristic of
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SOX9
No SOX9, no cartilage; and how DDRGK1 causes a rare human skeletal dysplasia
SEMD, Shohat-type spondyloepimetaphyseal dysplasia, is a rare type of skeletal dysplasia that affects the development of cartilage and results in a form of dwarfism with a
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