a mutation at the Xp21 locus on the X chromosome which results in the absence of the gene product dystrophin

Question Number 0777

Question:
Match the following mechanism or pattern with the appropriate disease: - a mutation at the Xp21 locus on the X chromosome which results in the absence of the gene product dystrophin

a) Rhabdomyolysis
b) Guillain-Barré syndrome
c) Charcot-Marie-Tooth
d) Duchenne muscular dystrophy
e) Becker muscular dystrophy


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