Answer:
Its is a lysosomal storage disease!
Explanation:
<u>Hurler syndrome:-</u> is also known as mucopolysaccharidosis-I .
It Is due to the mutation on chromosome 4 .
There is a lack of of enzyme called alpha-L-iduronidase.This enzyme is present in lysosomes
It causes accumulation of mucopolysaccharides because of the absent of the enzyme in the lysosome
<u>Hunter syndrome:- </u>is also known as mucopolysaccharidosis-II
It occurs due to mutation in iduronate-2-sulfatase (IDS) gene.It is an X-linked disease
Answer:
The answer is C (UAAGCUCGU)
Explanation:
T is replaced by U in RNA and A and U "bind". In this case, we're looking for the complementary RNA strand, so all terms are opposite; G becomes C, A becomes U, etc.
Evolutionary biologist hope this helps
Answer:
reading symbols or letters in a certain form,comparing information to figure out information
