A person affected with phenylketonuria l...

A person affected with phenylketonuria lacks an enzyme that converts the amino acid phenylalanine into :

Valine

Proline

Histidine

Tyrosine

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State True of False (i) Hetrozygous female for baemophilia may transmit the disease to sons (ii) Affected individuals with phenylketonuna lack an enzyme that converts the amino acid phenylalanine into phenylpyruvic acid (iii) Klinefelter's syndrome is caused due to the presence of an additional copy of X-chromosome resulting into a karyotype of 47//XXX (iv) Failure of segregation of homologous pair of chromosomes during cell division cyclic results in Turner's syndrome.

An individual affected by phenylketonuria lacks an enzyme that converts the amino acid "_____" into "_____"

An inborn error of metabolism in which the affected individual lacks an enzyme that converts aminoacid phenylalanine into tyrosine is

Which base triplets code for the amino acid phenylalanine ?

The enzyme that converts oxaloacetate into malic acid is

Assertion : Phenylketonuria, Haemophilia and sickle cell anemia are genetic disorders. Reason : In phenylketonuria the person has a non-functional enzyme for the conversion of phenylalanine to tyrosine.

The ezyme which changes amino acid phenylalanine to amino acid tyrosine is

Individuals suffering from phenylketonuria lack an enzyme required for the conversion of

An acidic amino acid is

What are acidic amino acids?

ARIHANT NEET-HUMAN GENETICS-Chapter Exercise (c) Medical entrances gallery (Collection of questions asked in NEET & Various Medical Entrance Exams)

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