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SLCO5A1 gene

Known as: SLCO5A1, solute carrier organic anion transporter family member 5A1, OATPRP4 
National Institutes of Health

Papers overview

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2017
2017
Mesomelia‐synostoses syndrome (MSS) is a rare, autosomal‐dominant, syndromal osteochondrodysplasia characterized by mesomelic…