In an individual with phenylketonuria,there is an enzyme deficiency. This enzyme converts phenylalanine into ........ .

  • A
    Glutamic acid
  • B
    Valine
  • C
    Tyrosine
  • D
    Tryptophan

Explore More

Similar Questions

$A$ normal woman,whose father was colour blind,marries a normal man. What is the chance of occurrence of colour blindness in the progeny (in $;\%$)?

What are the chances of colour-blind daughters and sons being born in a marriage between a normal man and a normal woman whose father was colour-blind?

$A$ person is suffering from the disease phenylketonuria, which is an autosomal recessive disease. Which of these is lacking in the person?

If a father and son are both defective in red-green colour vision,is it likely that the son inherited the trait from his father? Comment.

Match the following symbols used in Pedigree analysis:
Column-$I$ Column-$II$
$a.$ Solid symbol$(i)$ Carrier of sex-linked trait
$b.$ Horizontal line between symbols$(ii)$ Offspring
$c.$ Horizontal line above the symbols$(iii)$ Affected individual (Trait to be studied)
$d.$ Dot in centre$(iv)$ Mating (Parents)

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo