Phenylketonuria (PKU) || Phenylalanine Metabolism
Phenylketonuria - This video is on Phenylketonuria with NEET PG and AIIMS MCQS.
Phenylketonuria is an inborn error of phenylalanine metabolism, associated with the inability to convert phenylalanine to tyrosine because deficiency of Phenylalanine Hydoxylase enzyme.
Phenylketonuria is inherited as Autosomal recessive manner
It result in accumulation of phenylalanine in tissues and blood and its increased excretion in urine.
Видео Phenylketonuria (PKU) || Phenylalanine Metabolism канала Biochemistry Basics by Dr Amit
Phenylketonuria is an inborn error of phenylalanine metabolism, associated with the inability to convert phenylalanine to tyrosine because deficiency of Phenylalanine Hydoxylase enzyme.
Phenylketonuria is inherited as Autosomal recessive manner
It result in accumulation of phenylalanine in tissues and blood and its increased excretion in urine.
Видео Phenylketonuria (PKU) || Phenylalanine Metabolism канала Biochemistry Basics by Dr Amit
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27 февраля 2020 г. 14:21:25
00:12:48
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