Accepted
at 5:31 p.m. Feb, 03, 2025
by
andrewmathias8
Author:
andrewmathias8
Type of change:
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Rationale for change
full name with acronym
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- Due to association with congenital hepatic fibrosis
- ARPKD is due to a mutation in PKHD1 gene on chromosome 6, which codes for fibrocystin
- ARPKD is due to a mutation in PKHD1 gene on chromosome 6, which codes for fibrocystin
Lecture Notes
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Missed Questions
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Pathoma
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Boards and Beyond
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First Aid


Sketchy 2
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Sketchy Extra
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Picmonic
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Pixorize
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Physeo
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OME
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