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Type I tyrosinemia is a genetic pathology that gives rise to a very serious hepatic metabolic disease, above all because until now it has always been diagnosed after having found the symptoms. It is transmitted in an autosomal recessive manner , by a mutation on chromosome 15 , of the gene for the hydrolysis enzyme&hellip; Continua a leggere Type I tyrosinemia: today it is possible to diagnose it in time

Type I tyrosinemia: today it is possible to diagnose it in time | BioBlog

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