Sickle cellanaemia is is inherited
in an
autosomal recessive
Pattern
meaning
that both copies of the gene in
gene in each cell have mutations of GAG (normal) with
a GTG (sickle) codon. The parent of
individual with
autosomal recessive
condition each carry one copy of
mutated genes but they typically do not
carry one copy of gene,
whow signs and symptoms of
the condition. from the above statement
discuss in detail the best analytical technique to be used in detecting
the mutated gene in
the f1s of a
sickle cell population