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- Phenylketonuria
Images - Phenylketonuria
PKU Disease - Fenilketonurija
- Phenylketon
- Phenylketonuria
Defect - Phenylketonuria
Symptoms - Phenylalanine Hydroxylase
Deficiency - Phenylketonurie
- PKU Foods
to Avoid - Condition
Phenylketonuria - Phenylketonuria
Chromosome - Phenylketonuria
Babies - PKU
Mutation - Phenylketonuria
Logo - PKU
Child - Phenylketonuria
Chemistry - Phenylalanine Hydroxylase
Gene - Phenylketonuria
and Aspartame - Phenylalanine Metabolism
Pathway - Phenylalanine Amino
Acid Structure - Phenylketonuria
P - Neonatal
Tyrosinemia - Celebrities with
Phenylketonuria - Phenylalanine Hydroxylase
Reaction - BH4
Dopamine - Phenylalanine Hydroxylase
Enzyme - Physiopathologie De
La Phénylcétonurie - Thérapie Génique Pour
La Phénylcétonurie - Phénylcétonurie
Symptômes - Phenylketonuria
Urine Color - Phenylalanin
- Aspartame and
Phenylketonuria - Phenylketonuria
Cell - Gene
Defect - Phenylketonuria
Phenotype - Apolipoprotein
Types - Blood Test
Baby - PKU
Enfermedad - Phenylketonuria
Blue Eyes - Biochemistry of
Phenylketonuria - Phenylalanine
Model - Alkaptonurie
- Aminoacidos
- PKU Musty
Odor - Immunodeficiency
- Recessive Dystrophic
Epidermolysis Bullosa - Phenylalanine Hydroxylase
Structure - Trimetilaminuria
- Phenylketonurics
- Phenylalanine
Disease
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