Two types of heritable mutations are associated with FH; (1) a mutation in the NPXY signal sequence of the LDL receptor and (2)
a mutation in the adapter protein, AP2. Describe how each of the mutations results in disease g
1 answer:
I honestly don’t know, I just need to answer this so I can ask a question ⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️ ⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️ ⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️
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