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19 votes
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

User Jinesh Shah
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1 Answer

21 votes
21 votes
I honestly don’t know, I just need to answer this so I can ask a question ⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️ ⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️ ⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️⚪️
User Sam Mason
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