Matches in Nanopublications for { ?s ?p "[Phenylalanine hydroxylase (PAH) deficiency is caused by mutations in the PAH gene resulting in a primary deficiency of the PAH enzyme activity, intolerance to the dietary intake of phenylalanine (Phe), and production of the phenylketonuria disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_assertion description "[Phenylalanine hydroxylase (PAH) deficiency is caused by mutations in the PAH gene resulting in a primary deficiency of the PAH enzyme activity, intolerance to the dietary intake of phenylalanine (Phe), and production of the phenylketonuria disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_provenance.
- NP606454.RAXWu3MW7gkk9VseAmarhoz-NRxsW7hdCfvQyl_1gFmEY130_assertion description "[Phenylalanine hydroxylase (PAH) deficiency is caused by mutations in the PAH gene resulting in a primary deficiency of the PAH enzyme activity, intolerance to the dietary intake of phenylalanine (Phe), and production of the phenylketonuria disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606454.RAXWu3MW7gkk9VseAmarhoz-NRxsW7hdCfvQyl_1gFmEY130_provenance.
- NP796411.RAOgo_kG2W-D5BWdZ93A0yKYfFaHJW7JPmeVcAxjGi0EY130_assertion description "[Phenylalanine hydroxylase (PAH) deficiency is caused by mutations in the PAH gene resulting in a primary deficiency of the PAH enzyme activity, intolerance to the dietary intake of phenylalanine (Phe), and production of the phenylketonuria disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796411.RAOgo_kG2W-D5BWdZ93A0yKYfFaHJW7JPmeVcAxjGi0EY130_provenance.