चयापचय अनुवांशिक विकार, शरीरातील द्रवपदार्थांमध्ये एन्झाईमची कमतरता झोपेची गरज म्हणून ओळखली जाणे आवश्यक आहे, ज्यामुळे टायरोसिनचा परिणाम वेगवेगळ्या प्रमाणात मानसिक वंचितपणात होतो.,

Noun:

phenylketonurial च्या,

phenylketonuria's Usage Examples:

Individuals with phenylketonuria (PKU) must keep their intake of phenylalanine - an essential amino.

BioMarin was also the first company to provide therapeutics for phenylketonuria (PKU).

metabolism of nutrients, such as in lactase deficiency, phenylketonuria and favism.

It has been suggested that carriers of alleles associated with phenylketonuria may have been protected from spontaneous abortion caused by ochratoxin.

After phenylketonuria, glycine encephalopathy is the second most common.

An example of pleiotropy is phenylketonuria, an inherited disorder that affects the level of phenylalanine, an.

Also, BH4*2HCL is FDA approved for use in phenylketonuria (PKU), along with dietary measures.

syndrome, phenylketonuria, and Huntington disease and can be a feature of kernicterus (rapidly increasing unconjugated billirubin that cross the blood-brain-barrier.

caused by congenital disorders of amino acid metabolism, for example, phenylketonuria, or may be secondary to liver disease.

on account of their capacity for inducing hyperphenylalaninemia and phenylketonuria.

developing the bacterial inhibition assay used to screen infants for phenylketonuria at birth, before the development of irreversible neurological damage.

The genetic disorder phenylketonuria (PKU) is the inability to metabolize phenylalanine because of a lack.