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Top suggestions for Phenylalanine Hydroxylase Deficiency
Hyperphenylalaninemia
Phenylalanine Hydroxylase
17A
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Hyperphenylalaninemia
Phenylalanine Hydroxylase
17A
Hydroxylase Deficiency
Phenylalanine Hydroxylase
Reaction
Phenylalanine
Disease
Phenylalanine
Metabolism Pathway
Phenylketonuria
PKU Disease
Phenylalanine
Tyrosine Pathway
Phenylalanine Hydroxylase Deficiency
Symptoms
Low-Phenylalanine
Diet
PAH
Gene
Phenylalanine
Amino Acid
21-
Hydroxylase Deficiency
Phenylalanine Hydroxylase
Mechanism
Phenylalanine
Location
PAH mRNA
Sequence
Functional Groups of
Phenylalanine
Phenylalanine
Cycle
1-Alpha-
Hydroxylase
Metabolic Pathway of
Phenylalanine
Phenylalanine
and BH4
Phenylalanine Hydroxylase
Enzyme
PKU
Disorder
PKU Biochemical
Pathway
Lack of
Phenylalanine
PKU
Person
Hyperphenylalanemia
Types of
Phenylketonuria
PKU
儿童
Phenylalanine Hydroxylase
Cofactor
Phenylalanine
Neurotransmitter
Variants
of PKU
Phenylketonuria
بالعربي
Phenylalanine Hydroxylase
Mutation
Phenylalanine Hydroxylase
Liver
Deficiency of Phenylalanine
Hydrxylase Human
PKU
Patient
Hyperphenylalaninaemia
Phenylalanine
Alpha Carbon
Phenylalanine Deficiency
Kid
7A Hydroxlase
Deficiency
Phenylalanine
Hydroxylas Enzyme
Phenylalanine Hydroxylase
System
Phenylalanine Hydroxylase
Monomer
Phenylalanine Hydroxylase
or Tetrahydrobiopterin
Phenylalanine Hydroxylase Deficiency
Presentation
Cytometry of
Phenylalanine Hydroxylase
Maternal
Phenylketonuria
Phenylalanine Hydroxylase
Model
Phenylalanine Hydroxylase
Ribbon Diagram
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