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Phenylketonuria Genetic Disease Unable Break Phenylalanine Autosomal Recessive

Phenylketonuria is an autosomal recessive genetic disorder that prevents the breakdown of phenylalanine, causing its harmful accumulation.

Phenylketonuria is an autosomal recessive genetic disease where individuals cannot break down the amino acid phenylalanine, leading to its buildup.

Front Phenylketonuria
Back - genetic disease of being unable to break down phenylalanine
- autosomal recessive

Tags: chapter_09

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