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History (14)
Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia.
Phosphatidylcholine-Sterol O-Acyltransferase
A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2.
Drug delivery systems and materials for wound healing applications.
Antibacterial Fusion Proteins Enhance Moraxella catarrhalis Killing.
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Patrick McEnaney
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Busconi, Brian
Litwin, Demetrius
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Hernia
Athletic Injuries
Saphenous Vein
Hospital Costs
Heart-Assist Devices
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Busconi, Brian
Litwin, Demetrius
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