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Description
Wilson disease is an autosomal recessive disorder Autosomal recessive means that an affected individual inherits two copies of the disease-causing genetic mutation: one from their mother and one from their father, each of whom are considered carriers of the disease
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Surawski, N
However, the association between reduced chondrocyte quality during expansion and ACI outcome is less studied
Serum insulin was measured using an Ultra-Sensitive Mouse Insulin ELISA (CristalChem)
318 : 187193 Pawson T (1994) Introduction: protein kinases
