Tuesday, December 31, 2013

Phenylketonuria PKU

Phenylketonuria PKU Danielle Woods Genet 351, K. Owens Research paper Phenylketonuria: PKU Phenylketonuria also known as PKU once had irrevoc equal to(p) and detrimental damage to the disentangle sum it effected. Babies that were born with the genetic disorder were certain to stimulate from severe mental retardation and behavioral disorders be convey no star knew what was causation the symptoms. Until 1934 when a biochemist and doctor named A. Folling from Norway discovered the disease through and through water supply testing.
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(Mange,4) He identified that it was a familial disease which causes the stirred person’s body to non be able to handle a substance called phenylalanine (phe), an indwelling 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 sine qua non to get a full essay, order it on our website: BestEssayCheap.com

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