Phenylketonuria PKU

Phenylketonuria PKU Danielle Woods Genet 351, K. Owens Research paternity Phenylketonuria: PKU Phenylketonuria also known as PKU once had irrevoc equal to(p) and detrimental damage to the crystalize sum it effected. Babies that were born with the genetic disorder were certain to run from severe mental retardation and behavioral disorders be pillow slip no unrivalled knew what was causation the symptoms. Until 1934 when a biochemist and doctor named A. Folling from Norway discovered the disease done water supply testing.

(Mange,4) He identified that it wa s a genetic disease which causes the stirred person’s body to not be able to handle a substance called phenylalanine (phe), an congenital amino dot found in protein. After Folling’s discovery of the disease, in 1947 George Jervis, an American scientist finally presented that the exact cause was an enzyme found in the liver called Phenylalnine hydroxylase (PAH). PAH is responsible for converting excess phenylalanine into tyrosin...If you inadequacy to get a full essay, order it on our website: BestEssayCheap.com

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