Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia von Ansari, Hossein, Mohammadi‐Asl, Javad, Hajjari, Mohammadreza, Tahmasebi‐Birgani, Maryam, Kollaee, Abolghasem, Jassemi‐zergani, Farzad, Vakili‐Hajiagha, Amin

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